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Peptides

SAE Media Group is delighted to announce the 4th annual Peptides conference returning to London on the 6th - 7th July 2017, featuring two pre-conference workshops on the 5th July!

This information-packed 2-day conference will give you the perfect platform to network, collaborate and learn, featuring various key presentations by senior level industry professionals and Big Pharma speakers. Read our exclusive speaker interviews in the download centre to get an insight into what they have to say!


In the past few years, new technological advancements in the pharma industry have influenced the growth of the global peptide therapeutics market, which is now estimated to reach US $23.70 billion by 2020, with an increased number of peptides now in the pipeline of many biotech companies. Peptide manufacturers and suppliers have been developing and implementing new technologies to improve the peptide production, reduce manufacturing costs, and allow for more accurate formulations to enhance overall drug delivery.

 

Programme highlights include:

  • Spotlight on Liquid Chromatography / Mass Spectronomy as key techniques for Peptide Purification and applications for development and commercial peptides featuring case studies and examples, presented by Big Pharma speakers (Pfizer, Ferring, Ipsen, Novartis)
  • Strategies for Peptide Half-Life Extension including an update from the GLP-1 field and techniques on improving delivery of peptides, presented by Sanofi and Albumedix
  • Achieving Peptide Optimisation by improving physical and chemical Stability, Permeability and Bioavailability, presented by Pfizer, Sanofi and Bristol-Myers Squibb
  • Protein-Protein Interactions in Drug Discovery including library design and screening approaches, presented by VP of UCB and Head of IRBM Science Park

 

Previous attendee testimonials:

"Nice sized meeting and friendly! Plenty of opportunity to talk"

"The discussions and topics were diverse"

"Very interesting talks"

FEATURED SPEAKERS

Alastair Lawson

Alastair Lawson

Research Fellow, Vice President Structural Biology, UCB
Cecile Brocard

Cecile Brocard

Director Downstream Development, Boehringer Ingelheim
Craig Harris

Craig Harris

Head of Research Synthesis, Nestlé Skin Health
Elisabetta Bianchi

Elisabetta Bianchi

Head of Peptide Chemistry , IRBM Science Park

Alastair Lawson

Research Fellow, Vice President Structural Biology, UCB
Alastair Lawson

Alastair has been closely involved with the discovery of UCB/Celltech’s therapeutic antibodies, including Mylotarg, Cimzia, romosozumab, inotuzumab ozogamicin, dapirolizumab pegol, olokizumab, bimekizumab and UCB7665. Alastair led the development of UCB’s proprietary antibody variable region discovery platform, and is now applying structure-based, rational design to antibody discovery. He pioneered UCB’s small molecule protein/protein interaction initiative, in which information derived from antibodies is applied to the discovery and design of new chemical entities. Current research interests include the use of function-modifying antibody fragments to define specific conformations of target proteins, linking X-ray crystallography, molecular dynamics simulations and antibody technology to small molecule fragment screening.

Alessandro Butté

Lecturer, ETH Zürich
Alessandro Butté

Workshop Leader B

Alessandro Butté received his Ph.D. in Chemical Engineering in 2000 from ETH Zurich. After a two-year post-doc at the Georgia Institute of Technology, he join the group of Prof. Morbidelli at ETH Zurich and completed his habilitation in 2008. During this period, his research activities focused on polymer engineering, production of nano-materials for protein purification (monoliths by reactive-gelation) and chromatography purifications of peptides, proteins and Mabs. In 2008, he joined Lonza as leader for downstream activities in the sectors small molecules and peptides and as project manager. He was also involved in the pilot program to introduce Quality by Design into R&D. In 2013, he joined back ETH as senior researcher. His current main research area is focused on the use of big data, advanced statistics and machine learning in combination with classical mechanistic models for risk management in R&D and manufacturing of biomolecules. He is author of more than 60 papers on international peer reviewed journals and several book chapters.

Bhagyashree Khunte

Senior Principal Scientist, Pfizer
Bhagyashree Khunte

Bhagyashree Khunte is a Senior Principal Scientist in the R&D division at Pfizer Inc. with over 15 years of experience in separation sciences. She leads the high throughput singleton and library purification group that provides purification support to Medicinal Chemistry lines. Her work has included enhancing purification technologies to enable purification of beyond rule of five molecules including chemical probes, peptides, oligonucleotides, and protein and antibody drug conjugates.

Cecile Brocard

Director Downstream Development, Boehringer Ingelheim
Cecile Brocard

Cécile Brocard studied Biochemistry and Molecular Cell Biology in France, holds a PhD in Biochemistry from the University of Vienna (Austria) and has over 20-year experience in protein biochemistry.

Currently she is leading Downstream Development in Process Science at Boehringer Ingelheim Regional Center Vienna. As Head of Downstream Development she is responsible for DSP processes development for non-platform recombinant proteins expressed in microbial including, clinical supplies phase I/II/III and tech transfer to production. She heads a group composed of two downstream development units and a non-GMP pilot plant. Besides, she is critically involved in driving technology programs and strategic initiatives to develop innovation and improve process flows.

Craig Harris

Head of Research Synthesis, Nestlé Skin Health
Craig Harris

Dr. Craig Harris obtained his B.Sc. and Ph.D. at the University of Manchester (UMIST) in 1997. After a brief stay in PR&D at AZ, from 1999 he moved to Discovery Research working in the Oncology iMed for AZ working principally on kinase inhibition initially at the Alderley Park site then at the Reims site, France. After the closure of the Reims site in 2012, he was taken on as Head of Research Synthesis at for then Galderma (now, Nestlé Skin Health) Research Chemistry. In 2014, he was nominated as Senior Expert Scientist for Chemical Sciences.
During his career, he has won several prizes for publications and innovation in synthesis. Craig’s main interests lie in the word ‘Lean’ applied to chemical research: Rapid & selective synthesis of novel molecules for pharmacological targets. In addition to his background in the synthesis of novel kinase inhibitors as anti-cancer agents, Craig has developed a particular experience in the synthesis of peptidomimetics for targets in drug discovery.

David Price

Senior Director, Internal Medicine, Pfizer
David  Price

David A. Price currently holds the position of Senior Director in the Cardiovascular and Metabolic Diseases department within Pfizer. David obtained a B.Sc. (First Class Hons.) and Ph.D. from the University of Nottingham, UK, after which he carried out postdoctoral research at Colorado State University with Prof. Meyers. This work was directed towards the asymmetric synthesis of azasugars for the potential treatment of HIV. In 1998, David returned to the UK to take up a position as a Team Leader in Discovery Chemistry with Pfizer. In 2007, David transferred to Pfizer’s research headquarters in Groton, CT to assume a leadership role within the bone research group and then relocated to Cambridge MA to help lead the diabetes/obesity medicinal chemistry group. During his tenure with Pfizer, David has worked on projects to develop drugs for a wide variety of diseases including HIV/AIDS, respiratory diseases and, most recently, type II diabetes contributing to many clinical candidates that progressed to man. His most significant achievement has been the discovery of the marketed drug Maraviroc (Selzentry®), which received FDA approval in 2007 for the treatment of HIV infection.

Dieter Kadereit

Lab Head, Peptides & Insulins, IDD, R&D, Sanofi
Dieter Kadereit

Dieter Kadereit studied chemistry at the University of Hannover in Germany. After spending a year in Stanford, California with Prof. Wender he moved to the RWTH Aachen for his diploma research with Prof. Bolm and finally to the University of Karlsruhe for his PhD with Prof. Waldmann.
In the year 2000 Dieter joined Aventis as a laboratory head in chemistry. Soon he also became project team leader for his project and remained in that double role through several reorganizations and in different departments. Today he is working as laboratory head and project team leader in the Peptides & Insulins group in Sanofi’s Integrated Drug Discovery Research Platform.

Elisabetta Bianchi

Head of Peptide Chemistry , IRBM Science Park
Elisabetta Bianchi

Elisabetta Bianchi has been the Head of Peptide Chemistry at IRBM Science Park Pomezia (Italy) since 2010. In 2014 she obtained the Italian National Academic Qualifications as associate professor in Organic Chemistry and Molecular Biology. She started her career in the pharmaceutical industry in the Peptide Chemistry Group at Eniricerche followed by positions in Sclavo and Menarini Ricerche before joining IRBM in 1991. After full IRBM acquisition by Merck Research Laboratories in 2007 she was appointed Senior Investigator in the Peptide Center of Excellence at Merck. As project leader and member of Merck Early Development Teams she contributed to the preclinical and clinical development of peptide vaccines and peptide therapeutics. She is the author of 67 scientific publications in peer-reviewed journals and inventor in more than 30 patent applications.

Frank Thielmann

PMO & Operational Excellence Lead, Novartis
Frank Thielmann

Dr Thielmann graduated from University of Duesseldorf, Germany in 1996 with a diploma in Chemistry. This was followed by a PhD in Physical Chemistry in 1998 in the area of materials characterisation. Frank then worked for a private materials testing institute in Hannover, Germany before joining Surface Measurement Systems UK (SMS) in 2000. He stayed with SMS for eight years in different roles including global Head of Application Science. In this role, he was heavily involved in the development of novel characterisation methods for the challenges in the modern (bio)pharmaceutical industry with focus on solid dosage forms. Frank joined Novartis Pharma (Basel, Switzerland) in July 2007 as Formulation Lab Head. From August 2009 until February 2011 he managed the inhalation & device development group at the Horsham site, UK. Upon his return to Basel he took on the responsibility for the local inhalation technology platform until February 2012. Subsequently he joined Novartis Technical Operations where he was leading the setup of a new inhalation manufacturing facility and the transfer of the corresponding portfolio.
In December 2016 Frank joint the Biologics Technical Development & Manufacturing department as the Lead for PMO & Operational Excellence.
Dr Thielmann is member of the Steering Committee of the Material Science Focus Group in the British Academy of Pharmaceutical Sciences. He is an author and co-author of more than 25 articles in peer reviewed journals as well as author and co-author of more than 50 oral presentations at international conferences and seminars and over 100 scientific posters.

Joanna Hay

Science Manager, Albumedix
Joanna Hay

Joanna Hay obtained a B.Sc. in Biochemistry from the University of Birmingham (UK) and a Ph.D. in Biochemistry from University of Leicester. Joanna joined Albumedix in 2006 as a Scientist working with the R&D team on the development and optimization of engineered albumins for half-life extension technology, Veltis®. Currently Joanna is working as a Science Manager in Albumedix, working with drug developers wanting to evaluate the potential of the Veltis in their drug development programs.

John Reilly

Senior Research Investigator, Novartis Institutes for BioMedical Research
John Reilly

Chair for Day 1

Dr. Reilly is a Senior Research Investigator in the Department of Global Discovery Chemistry at Novartis Institute of Biomedical Sciences in Cambridge MA, USA. He currently leads the Chemistry Separations support team where there is a focus on providing purification and analytical characterization methodologies to support an expanding Chemistry unit. He completed both MSc. Birkbeck College in 1992 and Ph.D within Analytical Science Imperial College in 2002 after his initial BSc in Chemistry at Reading University in 1989. His research goals include the promotion of chromatographic characterization and purification methods and physicochemical affinity screens to investigate drug-like properties of molecules. Dr. Reilly has published >30 articles in many analytical journals such as J. Chromatography A, J. Med. Chem, J. Pharm. Biomed. Analysis, Chirality and Molecular Pharmacology. Dr. Reilly has been board member of the Chromatography Society in the UK and ChromSoc conference organiser and on the editorial board of “Chromatography Today” and “American Journal of Modern Chromatography.”

Jonathan Davis

Principal Scientist, Bristol-Myers Squibb
Jonathan Davis

Jonathan Davis received his Ph.D. from UC San Francisco, followed by a post-doc at Harvard Medical School in the labs of Jack Szostak and Gerhard Wagner. He then joined EMD Serono in Billerica, MA, where he invented a platform technology for generating heterodimeric Fcs and developed a novel scaffold based on an artificially-designed protein. He has extensive experience in selection technologies, library design, in silico modeling, and therapeutic discovery. In 2008 he moved to Bristol-Myers Squibb, where he is a Principal Scientists in Molecular Structure and Design, applying his skills to a wide range of challenges in protein and peptide engineering.

Jörgen Kjellgren Sjögren

Senior Research Scientist, Ferring Pharmaceuticals A/S
Jörgen Kjellgren Sjögren

Masters degree in Analytical Chemistry from Lund University, Sweden, in 1997 and PhD in Organic Chemistry from the Swedish University of Agricultural Sciences in Uppsala 2005. Worked with structure elucidation of peptides for >15 years utilising HPLC/UHPLC, MS and NMR and have >10 years experience of the pharmaceutical industry, 2½ years at Astra Zeneca, Lund, Sweden, and >11 years at Ferring Pharmaceuticals in Copenhagen, Denmark.

Lutz Jermutus

Senior Director & Product Development Team Leader, MedImmune
Lutz Jermutus

Chair for Day 2

.

Marie Skovgaard

Director Medicinal Chemistry, Zealand Pharma
Marie Skovgaard

Marie Skovgaard has an MSc in Biochemistry from University of Copenhagen, Denmark, and a PhD in Bioinformatics from the Danish Technical University. Marie started working with peptides during a PostDoc at Novo Nordisk before joining Zealand Pharma where she has been working with peptide drug development the past 10 years. Marie is currently heading up the Chemistry Department at Zealand Pharma. As Director of Chemistry she is responsible for overseeing peptide design and synthesis for the research pipeline.

Marion King

Analytical Development Manager, Ipsen
Marion King

Dr. Marion King is the Analytical Development Manager with Ipsen Manufacturing Ireland Ltd. She has over 13 years’ experience in the Pharmaceutical industry with 11 years working in the area of Analytical Development of peptides at Ipsen. Marion has a BSc in Analytical Chemistry from Cork Institute of Technology and a PhD from Dublin City University. Marion recently completed an MSc in Management and also leads a companywide Analytical Centre of Excellence (ACE) team. Marion is a member of the USP Biologics 1 – Peptides and Insulins Expert Committee and the JS3 Joint Subcommittee on biological reference standards.

Michal Bassani-Sternberg

Head of Immunopeptidomics Unit, CHUV and The Ludwig Cancer Institute
Michal Bassani-Sternberg

Michal Bassani-Sternberg received her PhD degree in Biology (2010) from the Technion - Israel Institute of Technology. From 2011 to 2015 she was a post-doctoral researcher at the Proteomics and Signal Transduction Department, headed by Prof. Matthias Mann at the Max Planck Institute of Biochemistry. She was awarded the Minerva and the Alexander von Humboldt fellowships. She developed mass spectrometry-based workflows for direct identification of HLA binding peptides eluted form tumor specimens and uncovered dozens of new cancer specific antigens including patient’s specific neo-antigens. Currently she is heading the Immunopeptidomics Unit and implements this technology in the Center of Experimental Therapeutics at the CHUV.

Roger New

Co-founder & CSO, Proxima Concepts Ltd
Roger New

Workshop Leader A

Roger New studied chemistry at Oxford and obtained a PhD in immunology at St Mary’s Hospital, London, before going to work in Liverpool for 14 years, first at the Department of Biochemistry, then at the School of Tropical Medicine and Hygiene. His research activities have centred on the creation of new technologies to improve the therapy of disease, during which time he has devised patented approaches to oral peptide delivery, vaccine carrier systems, and a technology for discovery of new therapeutics. He has acted as expert advisor in numerous institutions at home and overseas, has written a textbook on liposomes, and is honorary lecturer in Pharmaceutics at Kings College London. Dr New’s laboratory was the first to demonstrate the in vivo efficacy of liposomal amphotericin in leishmaniasis, a product which has now been commercialised for over ten years. He went into industry twenty years ago, first in Biocompatibles Ltd, then Cortecs, and is currently Co-founder and Executive Director of the biotech R&D company Proxima Concepts Ltd, with laboratories based in London. Development of the peptide delivery technology invented by Dr New has resulted in a product for oral administration of insulin, now in Phase II clinical trials, and licensed to large pharma in an emerging market. The discovery technology has yielded structures which can act as targeting agents, inhibit enzyme activity or change the behaviour of cells, and one peptide has been developed which is currently undergoing preclinical studies as a treatment for rheumatoid arthritis.

Vincent Bille

Managing Director, Marble Pharma Consult
Vincent Bille

Dr Vincent R. Bille is the founder and Managing Director of Marble Pharma Consult sprl, an independent firm offering consultancy services to pharmaceutical and biopharmaceutical companies that address all aspects of externalized process and analytical development as well as commercial manufacturing and testing activities.

Marble Pharma Consult has established a strong track record in international, cross-cultural project and relationship management and provides specific expertise in the areas of GMP-regulated primary and secondary pharmaceutical operations as well as regulatory-enabling activities including quality systems implementation, qualification and validation programs design and execution as well as the related technology transfers.

Prior to founding Marble Pharma Consult in 2007, Vincent served as Director Sales and Business Development for Lonza (Basel Switzerland), a global contract manufacturing organization. Before joining Lonza, Vincent held various operational and senior management positions with UCB-Bioproducts, a peptide CDMO subsidiary of the biopharmaceutical company UCB (Brussels, Belgium) including the positions of General Manager of the US subsidiary, Director Global Commercial Operations, Peptides and Formulation BU Manager and Operations and Development Manager.

Vincent Bille holds a Doctorate in Biochemistry (1987) and a Master’s Degree in Administration and Management (1994).

sponsors

Conference agenda

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8:30

Registration & Coffee

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9:00

Chairman's Opening Remarks

John Reilly, Senior Research Investigator, Novartis Institutes for BioMedical Research

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9:10

Antibody-enabled small molecule drug discovery

Alastair Lawson, Research Fellow, Vice President Structural Biology, UCB

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9:45

Understanding the Structure Activity Relationship of the Nrf2-KEAP1 protein-protein interaction site using an Nrf2-neh2 peptide library design approach

Elisabetta Bianchi, Head of Peptide Chemistry , IRBM Science Park

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10:20

Morning Coffee

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10:50

Synthesis of novel peptidomimetic inhibitors of Caspase I

Craig Harris, Head of Research Synthesis, Nestlé Skin Health

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11:25

Combinatorial Peptide Nanotechnology for Drug Discovery

Roger New, Co-founder & CSO, Proxima Concepts Ltd

  • Peptide nondomains
  • Receptor agonists
  • A priori drug discovery
  • From test tube to whole organism

     

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    12:00

    Networking Lunch

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    13:10

    Optimizing Permeability and Bioavailability of Peptide Macrocycles

    David Price, Senior Director, Internal Medicine, Pfizer

  • Prospective design of cell permeable macrocycles
  • Use of biophysical techniques
  • Future directions

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    13:45

    Fusion Strategy for the Recombinant Expression of Therapeutic Peptides in Microbial

    Cecile Brocard, Director Downstream Development, Boehringer Ingelheim

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    14:20

    From peptide lead candidate to pharmaceutical drug product

    Vincent Bille, Managing Director, Marble Pharma Consult

  • Process development, scaling-up and validation
  • Characterisation and process validation
  • Specifications and registration
  • Specific challenges associated with contract manufacturing service providers

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    14:55

    Afternoon Tea

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    15:25

    High Throughput Purification and Characterization of Peptides Using LC/MS/ELSD Techniques

    Bhagyashree Khunte, Senior Principal Scientist, Pfizer

  • Peptide QC
  • Purity analysis using LC/MS/ELSD techniques
  • Peptide purification
  • High Throughput purification workflow
  • clock

    16:00

    LC-MS a key technique to understanding the fate of impurities in Ferring’s synthetic therapeutic peptides

    Jörgen Kjellgren Sjögren, Senior Research Scientist, Ferring Pharmaceuticals A/S

  • LC-MS a great tool to understand fate of impurities
  • Separation is crucial as well as identification of impurities
  • Identification of impurities originating from starting material, synthesis, purification and degradation of peptides
  • Examples from Ferring’s synthetic peptide portfolio

     

  • clock

    16:35

    Mass-spectrometry based immunopeptidomics for personalised cancer immunotherapy

    Michal Bassani-Sternberg, Head of Immunopeptidomics Unit, CHUV and The Ludwig Cancer Institute

  • Biochemical extraction of HLA binding peptides form tumour tissues
  • Advanced mass-spectrometry analyses for identification and validation of HLA binding peptides
  • Immunopeptidomics in combination with genomics for identification of clinically relevant neo-antigens 
  • Prioritisation of tumour antigens for vaccination

     

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    17:10

    Chairman’s Closing Remarks and Close of Day One

    John Reilly, Senior Research Investigator, Novartis Institutes for BioMedical Research

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    8:30

    Registration & Coffee

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    9:00

    Chairman's Opening Remarks

    Lutz Jermutus, Senior Director & Product Development Team Leader, MedImmune

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    9:10

    Recent Progress in the Development of Once-Weekly GLP-1 Receptor Agonists

    Dieter Kadereit, Lab Head, Peptides & Insulins, IDD, R&D, Sanofi

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    9:50

    Extending Drug Half-Life to Achieve Monthly Dosing? The Potential of Veltis® Engineered Albumins for Optimised Dosing

    Joanna Hay, Science Manager, Albumedix

  • Short circulatory half-life represents a major obstacle for many peptide-based therapeutics
  • This can be significantly improved by conjugation or fusion to albumin, due to increased size and recycling via the neonatal Fc receptor (FcRn)
  • The increased FcRn affinity of the Veltis® engineered albumins translates to more than doubling of the already long half-life of native sequence albumin
  • We will describe rationally engineered albumins and their application to improve delivery of peptides

  • clock

    10:30

    Morning Coffee

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    11:00

    From challenging peptide to drug candidate – the dasiglucagon story

    Marie Skovgaard, Director Medicinal Chemistry, Zealand Pharma

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    11:40

    Peptides in the biopharmaceutical industry today and tomorrow

    Frank Thielmann, PMO & Operational Excellence Lead, Novartis

  • Small versus big molecules – benefits and differences in development & manufacturing of peptides
  • Industrial pipelines and disease areas addressed by biotherapies
  • NBEs versus NCEs
  • Future trends in manufacturing
  •  

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    12:20

    Networking Lunch

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    13:30

    Conquering a peptide optimisation challenge using protein engineering techniques and deliberate potency reduction

    Jonathan Davis, Principal Scientist, Bristol-Myers Squibb

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    14:10

    ReadyFlow - a first in class coagulant for controlling surgical bleeding

  • Unmet needs in the control of surgical bleeding and key factors to determine success
  • HX-P12 peptide: a first in class peptide coagulant
  • Design of a particulate hydrogel formulation
  • Current ReadyFlow formulation; challenges and progress

  • clock

    14:50

    Afternoon Tea

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    15:20

    The use of high resolution mass spectrometry applications for both development and commercial peptides

    Marion King, Analytical Development Manager, Ipsen

  • Mass Spectrometry of peptides that involve ligation technologies
  • Mass Spectrometry for confirming the removal of solid phase coupling reagents
  • Mass Spectrometry for impurity identification in life cycle management activities

     

  • clock

    16:00

    Purification, Characterization and Physicochemical Properties of Peptides within Discovery Chemistry

    John Reilly, Senior Research Investigator, Novartis Institutes for BioMedical Research

  • Chromatographic purification strategies for cyclic and linear peptides including SFC, LC and Flash methodologies
  • Stoichiometry of final salt forms using Ion Chromatography
  • Extraction strategy to remove TFA from final products
  • Physicochemical Trend Analysis on final products

     

  • clock

    16:30

    Chairman’s Closing Remarks and Close of Day Two

    Lutz Jermutus, Senior Director & Product Development Team Leader, MedImmune


    Research Fellow, Vice President Structural Biology
    UCB
    Lecturer
    ETH Zürich
    Senior Principal Scientist
    Pfizer
    Director Downstream Development
    Boehringer Ingelheim
    Head of Research Synthesis
    Nestlé Skin Health
    Senior Director, Internal Medicine
    Pfizer
    Lab Head, Peptides & Insulins, IDD, R&D
    Sanofi
    Head of Peptide Chemistry
    IRBM Science Park
    PMO & Operational Excellence Lead
    Novartis
    Science Manager
    Albumedix
    Senior Research Investigator
    Novartis Institutes for BioMedical Research
    Principal Scientist
    Bristol-Myers Squibb
    Senior Research Scientist
    Ferring Pharmaceuticals A/S
    Senior Director & Product Development Team Leader
    MedImmune
    Director Medicinal Chemistry
    Zealand Pharma
    Analytical Development Manager
    Ipsen
    Head of Immunopeptidomics Unit
    CHUV and The Ludwig Cancer Institute
    Co-founder & CSO
    Proxima Concepts Ltd
    Managing Director
    Marble Pharma Consult

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    Past Attendee List - Peptides 2016

    Download

    An interview with John Reilly, Senior Research Investigator for Novartis Institutes for Biomedical Research

    Download

    An Interview with Jörgen Kjellgren Sjögren, Senior Research Scientist, Ferring

    Download

    An interview with Craig Harris, Head of Research Synthesis, Nestlé Skin Health

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    Sponsors and Exhibitors


    Bachem

    Sponsors and Exhibitors
    http://www.bachem.com/

    Bachem provides comprehensive services to the pharma and biotech industries. It specializes in the development of innovative, efficient manufacturing processes and the reliable production of peptide-based APIs. The group has a global reach with more experience and know-how than any other company in the industry. Bachem. Pioneering Partner for Peptides


    PolyPeptide

    Sponsors and Exhibitors
    http://www.polypeptide.com

    The PolyPeptide Group is a world leading peptide drug substance manufacturer with six manufacturing facilities distributed over 5 countries and 3 continents (Belgium, France, India, Sweden, USA). Our exclusive focus on peptides for pre-clinical, clinical and commercial use provides our customers with the highest quality products and services that exceed expectations.


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    Tepnel Pharma Services is an independent Contract Research Organisation which supports the drug development pipeline at the Rx/Dx interface. With over 30 years of experience in supporting pharmaceutical, biopharmaceutical and biotechnology companies through the provision of outsourced cGMP compliant Chemistry, Manufacturing and Control (CMC) and human genetics testing, Tepnel Pharma Services is positioned to provide CMC support for drug development, whilst also providing a companion diagnostic solution which addresses the requirements of personalised and stratified medicines.

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    IJCBDD, an International Society of Intelligent Biological Medicine official journal, bridges the gap between two very important, complementary disciplines, computational biology and drug design. Through advances in high-throughput genome sequencing and digital imaging technologies, biocomputing, drug design and medical research have unfolded new, predictive sciences such as genomics, proteomics, lipidomics, metabolomics, cytomics and pharmaconomics. These promote new computational, statistical and biomedical approaches to drug design/development, besides unleashing the potential of significantly more accurate, effective personalised diagnosis, therapeutics and patient care.


    International Journal of Biomedical Engineering and Technology

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    IJBET addresses cutting-edge research in the multi-disciplinary area of biomedical engineering and technology. Medical science incorporates scientific/technological advances combining to produce more accurate diagnoses, effective treatments with fewer side effects, and improved ability to prevent disease and provide superior-quality healthcare. A key field here is biomedical engineering/technology, offering a synthesis of physical, chemical, mathematical and computational sciences combined with engineering principles to enhance R&D in biology, medicine, behaviour, and health. IJBET includes the Asia-Pacific Chapter in Biomedical Wireless Technology (APC-BWT).


    Farmavita

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    FarmavitaR+ is the professional network of experts and service providers. Network is gathering local consultants from 90 countries in Europe, Asia, North America, Latin America, Australia and Africa. Management of international, multi-centre projects is our core competence. FarmavitaR+ is providing solutions related to pharmaceutical, medical device, food supplement and cosmetic products. Scope of services is related to solutions for product development, quality assurance, clinical trials, product registration, portfolio analysis, lifecycle management, vigilance/risk management, pricing/reimbursing, market access and promotional compliance. FarmavitaR+ is brand name of Farmavita Regulanet Ltd. Visit https://farmavitar.com for more information. Outsource anything you can think of!


    Labiotech.eu

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    Labiotech.eu is the leading digital media covering the European Biotech industry. Over 100,000 monthly visitors use it to keep an eye on the business and innovations in biotechnology. Hope you'll enjoy reading our stories!


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    BioChem Adda is a Not-just-for-Profit organization which aims to bring out the most reliable and transparent information about everything related to jobs, careers, education, news, articles, and events from the field of BioSciences and Chemistry!


    International Journal of Biotechnology

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    IJBT provides an international forum and refereed authoritative source of information in the field of Biotechnology and Biotechnics, with emphasis on management and economics, as well as the political and social issues. It aims to disseminate knowledge, provide a learned reference in the field, and establish channels of communication between academic and research experts, policy makers and executives in industry, commerce and investment institutions.


    International Pharmaceutical Industry

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    IPI gives you an insight into all areas of Biopharm, Medical, Pharmaceutical and Healthcare. IPI provides a proven supportive means of communication to the Pharmaceutical, Bio Pharmaceutical, Nutraceutical and Medical Devices industry, incorporating the latest in research and technology innovations, regulatory guidelines, marketing and communication strategies.


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    GBI is an information, applications, and services company focused on the healthcare industry. Leveraging data from across the healthcare value chain, GBI creates web and mobile applications that enable individuals and organizations to make better decisions and communicate more effectively.


    Medical News Today

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    Medical News Today is the largest independent medical and health news site on the web - with over 10,000,000 monthly unique users it is ranked number one for medical news on all major search engines. Medical News Today is used by pharmaceutical, biotech and health organizations, advertising agencies, PR companies and vertical ad networks to deliver targeted campaigns to HCPs, patients and caregivers. To find out how Medical News Today can help you to reach the right audience contact peter@medicalnewstoday.com or visit www.medicalnewstoday.com.


    Swiss Biotech Association

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    The Swiss Biotech Association (SBA) is the national industry association for biotechnology, including pharmaceuticals, diagnostics, agriculture, food, cosmetics, environmental biotechnology, and specialty chemicals. Members are companies active in modern biotechnology, such as R&D, Production, Marketing and Sales, Finance, Services and Consulting. SBA provides a networking platform for Life Science clusters, academic and federal institutions the like. Founded in March 1998, the Association grows steadily.


    Pharmalicensing

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    Pharmalicensing (www.pharmalicensing.com) is the premier biopharmaceutical Open Innovation resource designed for professionals involved with partnering, licensing and business development worldwide. Actively supporting all forms of partnering and in- and out-licensing activities, Pharmalicensing utilizes the unique online Showcase Profiling & Discover services, as well as its renowned Partnering Search service leveraging its global network of industry experts, to enable companies to identify and engage with appropriate partners around the world. Pharmalicensing is actively utilized by many tens of thousands of industry professionals each month. Pharmalicensing is a division of Cognis Group, Inc.


    Select Science

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    SelectScience is an independent, online information resource for the worldwide scientific community, and the home of trusted information for laboratory scientists. Discover impartial, expert opinion and trusted reviews about latest laboratory equipment and techniques; plus videos, application notes and science news from around the world. Become a member for free today.


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    Biosave.com brings together the best Life Science promotions, product releases, featured products, publications, videos and events from 100’s of leading Life Science suppliers. Updated 24 hours a day, Biosave is constantly uploading special promotions and exciting product news that you won’t find anywhere else. Our goal is to provide our users with the most exclusive product information to help reach that all important purchasing decision.


    CanBiotech

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    CanBiotech - A Portal and B2B Outsourcing Marketplace for the Biotech and Pharmaceutical Industry. The Marketplace features the Outsourcing Services Showcase; the Portal features our biopharmaceutical and venture capital directories and databases. Publications include the BioMedical Outsourcing Report and the Bio Outsourcing Asia© Publication.


    Gate2Biotech

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    Gate2Biotech is a portal that unites biotechnological community in Central Europe. It covers all the news in the field of biotechnology. Thanks to the the portal the companies engaged in the field can easily search for research institutions and other partners to solve technical problems they are facing and here they can also present their services offer to potential partners from the Czech Republic and abroad. Gate2Biotech portal serves as a bridge connecting scientific and commercial sector. It incorporates offices and support organizations dedicated to promoting transfer of innovative technologies into a unified communication platform of Czech and international biotechnologies. As a mediator of information it draws attention to biotechnologies and support of their application and transfer into practice. It also functions as a tool for encouraging non-professionals (especially scientists and students) towards innovative business or applied research.


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    Founded in 2000, Technology Networks is established as the leading news provider for life science and drug discovery professionals. In addition, we provide unique content including webcasts, videos, application notes and posters from recent conferences. Our portfolio now includes around 30 focussed scientific communities, all of which are accessible free of charge within TechnologyNetworks.com


    Drug Discovery Today

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    Drug Discovery Today covers the whole of the preclinical drug discovery process. The reviews are cutting edge, written by experts in their respective fields and cover all aspects of drug discovery from genomic and proteomic approaches, computational drug design, medicinal chemistry and the translation of these sciences to therapies.


    Pharmaceutical-Review

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    Pharmaceutical-review.com is part of Integrated IQ technologies Private Limited(IIQ). A Leading platform for all the Pharma manufacturing companies and buyers across the world.Having a subscriber database of more than 120,000 globally helping the clients to reach their target buyers through our exclusive listing, branding(banner advertisement), e-news letters, e-mail marketing, product reviews, product launch promotions, event marketing, search engine marketing and social media marketing services.


    Drug Target Review

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    http://www.drugtargetreview.com

    Drug Target Review’s quarterly magazine, website and annual events program provides high quality content with peer-written articles that are submitted exclusively by the world’s most respected scientists in their field. This attracts a committed base of readers, users and delegates made up of senior decision-makers from the life science and drug discovery industries at the top pharmaceutical companies, as well as academics and scientists from the top research institutes across the globe.


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    Holiday Inn Kensington Forum

    97 Cromwell Road
    London SW7 4DN
    United Kingdom

    Holiday Inn Kensington Forum

    Holiday Inn Kensington Forum is perfectly situated in one of London’s most luxurious and beautiful areas within South Kensington. 

    The hotel is just 2 minutes walk from Gloucester Road tube station for convenient travel to Hyde Park, London Eye, Tower Bridge plus more of London’s top attractions. There are also easy and direct links to some major transport hubs including Victoria, Kings Cross St Pancras, Paddington and Heathrow. 

    This distinctive hotel in south London has so much to offer to make all guests really feel at home. The latest Holiday Inn relaunch is not just about the new look and feel for the hotel but to offer guests more benefits during their stay including a pillow menu for extra comfort during their sleep and a curved shower rail for more spacious feel. 

    In addition to our 906 rooms, all business guests can take advantage of our meeting and conference facilities including High Speed Internet Access and unlimited Starbucks coffee at The Academy. Our hotel’s professional event planners are on board to help take the hard work and stress away from planning your next event. 

    So whether you in London on business or pleasure, make the Holiday Inn London Kensington Forum your first choice of hotel and book your accommodation for our lowest internet rate guarantee. 

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    WHAT IS CPD?

    CPD stands for Continuing Professional Development’. It is essentially a philosophy, which maintains that in order to be effective, learning should be organised and structured. The most common definition is:

    ‘A commitment to structured skills and knowledge enhancement for Personal or Professional competence’

    CPD is a common requirement of individual membership with professional bodies and Institutes. Increasingly, employers also expect their staff to undertake regular CPD activities.

    Undertaken over a period of time, CPD ensures that educational qualifications do not become obsolete, and allows for best practice and professional standards to be upheld.

    CPD can be undertaken through a variety of learning activities including instructor led training courses, seminars and conferences, e:learning modules or structured reading.

    CPD AND PROFESSIONAL INSTITUTES

    There are approximately 470 institutes in the UK across all industry sectors, with a collective membership of circa 4 million professionals, and they all expect their members to undertake CPD.

    For some institutes undertaking CPD is mandatory e.g. accountancy and law, and linked to a licence to practice, for others it’s obligatory. By ensuring that their members undertake CPD, the professional bodies seek to ensure that professional standards, legislative awareness and ethical practices are maintained.

    CPD Schemes often run over the period of a year and the institutes generally provide online tools for their members to record and reflect on their CPD activities.

    TYPICAL CPD SCHEMES AND RECORDING OF CPD (CPD points and hours)

    Professional bodies and Institutes CPD schemes are either structured as ‘Input’ or ‘Output’ based.

    ‘Input’ based schemes list a precise number of CPD hours that individuals must achieve within a given time period. These schemes can also use different ‘currencies’ such as points, merits, units or credits, where an individual must accumulate the number required. These currencies are usually based on time i.e. 1 CPD point = 1 hour of learning.

    ‘Output’ based schemes are learner centred. They require individuals to set learning goals that align to professional competencies, or personal development objectives. These schemes also list different ways to achieve the learning goals e.g. training courses, seminars or e:learning, which enables an individual to complete their CPD through their preferred mode of learning.

    The majority of Input and Output based schemes actively encourage individuals to seek appropriate CPD activities independently.

    As a formal provider of CPD certified activities, SAE Media Group can provide an indication of the learning benefit gained and the typical completion. However, it is ultimately the responsibility of the delegate to evaluate their learning, and record it correctly in line with their professional body’s or employers requirements.

    GLOBAL CPD

    Increasingly, international and emerging markets are ‘professionalising’ their workforces and looking to the UK to benchmark educational standards. The undertaking of CPD is now increasingly expected of any individual employed within today’s global marketplace.

    CPD Certificates

    We can provide a certificate for all our accredited events. To request a CPD certificate for a conference , workshop, master classes you have attended please email events@saemediagroup.com

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    Contact SAE Media Group

    UK Office
    Opening Hours: 9.00 - 17.30 (local time)
    SAE Media Group , Ground Floor, India House, 45 Curlew Street, London, SE1 2ND, United Kingdom
    Tel: +44 (0) 20 7827 6000 Fax: +44 (0) 20 7827 6001
    Website: http://www.smgconferences.com Email: events@saemediagroup.com
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