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Regulatory challenges at the interface of medicines and medical devices
17 January 2017
Regulatory challenges at the interface of medicines and medical devices

This half day workshop will explore the challenges that both companies and regulators face when preparing and reviewing submissions for medicinal products incorporating a medical device – challenges that will likely increase as combination products become more complex. Furthermore, the new EU Medical Device Regulations will introduce a requirement for review of device components by notified bodies; the workshop will consider how this could work, and what data and supporting information should be provided for MAA submissions.

Workshop LEADER

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Janine Jamieson

ex-MHRA Assessor,

Janine has worked as a pharmaceutical assessor in the Medicines and Healthcare products Agency for over 18 years and over the last 10 years has developed an interest and focussed on products combining both medicines and medical devices. Through this role and participation in conferences, she has learned about the challenges at the interface of two quite different regulatory systems – and the need for collaboration to work towards pragmatic, risk based and proportionate regulation of such combination products.

Workshop agenda

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13:30

Workshop registration & welcome coffee

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14:00

Workshop leader introduction

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14:15

EU regulatory developments - MHRA update

•             EU developments on drug and biological/device combination products
•             Current data requirements and questions to expect
•             Future perspectives with increasingly complex combinations and impact of new Medical Device Regulations

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14:45

Interactive session – how can device manufacturers best support pharma in providing the most applicable data for MAA submission?

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15:30

Afternoon Tea & Networking Break

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16:00

Regulatory challenges in a global environment

•             Case study One - same product different regulatory requirements in different regions
•             Experience of questions asked and challenges overcome
•             Industry view on how to involve notified bodies in assessment of integral device components
 

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16:30

Discussion with all participants on the case study with different approaches and experiences

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17:00

Cross-Industry initiatives to address development and licensing of biologics/device combination products

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18:00

Closing remarks from Workshop leader and end of afternoon workshop

Holiday Inn Kensington High Street

Wrights Lane
Kensington
London
United Kingdom

Holiday Inn Kensington High Street

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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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