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SMi presents its 15th annual Parallel Trade virtual conference and workshop, taking place on the 24th March 2021. As the only parallel trade conference in Europe, this event provides the perfect platform for industry experts from both sides of the coin to come together and share perspectives on the practice of parallel trade.
 

Parallel trade within the EEC, EC, EU and EEA has been driven by the law on the free movement of goods and the single market imperative as applied under competition law. Disputes over pharmaceuticals have been a primary focus of the case-law, which has developed into a specialist area which can seem impenetrably complex. This workshop will demystify the law and provide some key touchpoints both for the current law and how it is likely to develop in reaction to new challenges.
 

• Clear overview of the legal framework, whether as an introduction or refresher
• Practical and applied sessions using case studies
• Interactive workshop led by well-established practitioners
• Key takeaways of the Covid-19 and Brexit impact on the field
 

Vice President/ Heads of/General Managers:
• International Trade and Relations
• Supply Chain Development – Brexit
• Brexit Implementation
• Market Access
• Supply Chain Manager
• Parallel trade reporting
• Regulatory Affairs
• IP
• Purchasing
• Policy Patent Operations
• European Affairs
• Supply and Demand
• Attorney
• Distribution

 

AbbVie; AIFA - Agenzia Italiana Del Farmaco; Amgen Europe BV; Arnold & Porter; Baker & Mckenzie; bij CyTuVax b.v. ; Bristows LLC; Covington & Burling; Daiichi Sankyo Europe GmbH; Department of Health and Social Care; EAEPC; Erasmus University Rotterdam; Europe Economics; European Alliance for Access to Safe Medicines; European Association of Euro-Pharmaceutical Companies ; Ferring Pharmaceuticals; FERRING SA; Freshfields Bruckhaus Deringer LLP; Gilead Sciences Ltd; Hollister Europe Ltd; Intellectual Property Office; IQVIA; IQVIA Commercial GmbH & Co. OHG; Key Pharmaceuticals Ltd; Kopinke; LEO Pharma; Lisman Legal Life sciences B.V.; Medac GmbH; MHRA; MSD Animal Health ; Mundipharma; Novartis Pharma AG; Novartis Pharmaceuticals UK Ltd; Novo Nordisk Bioindustrie Sa; Novo Nordisk Ltd; SoftGroupáLtd.; UEA, University of East Anglia; White & Case LLP; Wiggin LLP; Windt Le Grand Leeuwenburgh;
 

Workshop programme

9:00 Opening Remarks

9:10 Intellectual Property and Free Movement

• Exhaustion of rights
• Repackaging of pharmaceuticals: the BMS conditions
• Recent case law and case study
 

Christopher Stothers

Christopher Stothers, Partner, Freshfields Bruckhaus Deringer LLP
View Bio

Sharon Malhi

Sharon Malhi, Antiturst, Competition and Trade, Freshfields Bruckhaus Deringer LLP

9:50 Competition Law

• Anti-competitive agreements and dominant positions
• Quotas and direct-to-pharmacy models
• Recent case law and case study
 

Christopher Stothers

Christopher Stothers, Partner, Freshfields Bruckhaus Deringer LLP
View Bio

Sharon Malhi

Sharon Malhi, Antiturst, Competition and Trade, Freshfields Bruckhaus Deringer LLP

10:30 Morning Coffee

11:00 Regulatory Law

• Marketing authorisations
• Parallel import licences
• Recent case law and case study
 

Christopher Stothers

Christopher Stothers, Partner, Freshfields Bruckhaus Deringer LLP
View Bio

Sharon Malhi

Sharon Malhi, Antiturst, Competition and Trade, Freshfields Bruckhaus Deringer LLP

11:40 Covid-19 and Brexit

• How did Covid-19 affect the rules?
• How has Brexit affected the rules?
• Case study
 

Christopher Stothers

Christopher Stothers, Partner, Freshfields Bruckhaus Deringer LLP
View Bio

Sharon Malhi

Sharon Malhi, Antiturst, Competition and Trade, Freshfields Bruckhaus Deringer LLP

12:20 Closing Remarks

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FEATURED SPEAKERS

Christopher Stothers

Christopher Stothers

Partner, Freshfields Bruckhaus Deringer LLP

Christopher Stothers

Partner, Freshfields Bruckhaus Deringer LLP
Christopher Stothers

Christopher is a recognized expert in parallel trade, with a particular focus on the pharmaceutical sector - his 2007 textbook, “Parallel Trade in Europe: Intellectual Property, Competition and Regulatory Law,” has been cited by the UK Supreme Court. Christopher is also an experienced litigator on cross-border patent disputes, other types of intellectual property, antitrust, pharmaceutical regulation, EU law and commercial disputes. He has taken cases before the First Tier Tribunal, the Upper Tribunal, the Patents County Court, the High Court, the Court of Appeal, the House of Lords, the Supreme Court, the European Patent Office, and the European Court of Justice.
 

VENUE

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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, SMI 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@smi-online.co.uk

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