EU Pharmaceutical Regulations & Strategy

This course will provide an up-to-date overview of the European pharmaceutical regulatory environment, procedures and obligations.

31 Oct-1 Nov 2019

& 20-21 Apr 2020

GBP 1,499
EUR 2,099
USD 2,338

Book now

Course Overview

This course will provide an up-to date overview of the European pharmaceutical regulatory environment, procedures and obligations. You will learn about the legal basis of regulation, development strategies and the strategic importance of pre-submission actions, the format for presentation of data, how the registration procedures work and post-authorisation strategies and obligations.

It will be of value for regulatory affairs personnel and also for those who interact with regulatory personnel in order to understand action timelines and information requirements.

Benefits of attending:

  • Understand the legal basis of the EU regulatory environment
  • Discuss development strategy and pre-submission activities
  • Review procedures for applying for an EU marketing authorisation
  • Discuss post-authorisation strategic considerations and obligations

Who should attend?

This course will be of particular relevance if you are involved in:

• Regulatory affairs
• Project management
• Business planning
• Commercial management
• Manufacturing and QA
• Labelling and artwork
• Medical information
• Clinical
• Pharmacovigilance

Programme day one

EU regulatory environment: legal basis

  • Key regulations, directives and guidelines and information sources
  • Impact of Brexit

Development strategy and pre-submission activities

  • Scientific advice
  • Paediatric use

Case study 1: Submission requirements

The Common Technical Document (CTD)

  • Structure and content of the CTD

The EMA

  • Impact of Brexit

Applying for a marketing authorisation in the EU

  • Fast-track, conditional approval and exceptional circumstances
  • Adaptive licensing
  • Co-ordination group
  • Centralised Procedure (CP)

Case study 2: Registration strategy discussion

  • Will Brexit alter this?

Programme day two

Registration procedures

  • Decentralised Procedure (DCP)
  • Mutual Recognition Procedure (MRP)
  • National procedures

Managing product labelling

  • Company core data sheets
  • Updates to SmPC

Abridged applications

  • Legal basis
  • Data exclusivity
  • Generics – definition and criteria

Post-authorisation obligations and strategic considerations

Safety reporting

  • Pharmacovigilance

Licence variations

  • Type I and Type II variations

Strategic considerations

  • Line extensions
  • Classification switch
  • Parallel trade (impact of Brexit)
  • Phase IV studies

Case study 3: Post-authorisation strategy discussion

  • Will Brexit alter this?

Licence renewals

  • PSURs/PBRERs
  • The sunset clause

Presenter

Norah Lightowler (31 Oct-1 Nov 2019)

Norah Lightowler is a partner in Lightowler Associates, an independent consultancy offering regulatory advice and support to pharmaceutical companies in or proposing to enter the European market for human pharmaceuticals. They are in their twenty fourth year of successful business. She has wide experience in the pharmaceutical and related nutraceutical, herbal and devices industries as a pharmaceutical assessor with the UK regulatory authority and as associate director of European regulatory affairs with an international pharmaceutical company. She is experienced in organising and presenting courses on European regulatory control systems, including requirements, procedures and strategy.

Book now

31 Oct-1 Nov 2019
31 Oct-1 Nov 2019 Rembrandt Hotel, London GBP 1,499.00
EUR 2,099.00
USD 2,338.00
+ VAT @ 20.00%
Enrol now
20-21 Apr 2020
20-21 Apr 2020 Venue not yet confirmed
+ VAT @ 20.00%
Online registration unavailable: this date is nearing full capacity; please call us on 020 7749 4730 to register.

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Previous customers include...

  • Acino Pharma AG
  • Agency for Medicinal Products and Medical Devices
  • AOP Orphan Pharmaceuticals
  • Aspen Pharma Trading Limited
  • BELUPO Pharmaceuticals & Cosmetics Inc
  • Boots Management Services Ltd
  • Chiesi Farmaceutici S.p.a.
  • Convergence Pharmaceuticals
  • GALDERMA Recherche & Developpement
  • Galderma S.A.
  • HRA Pharma UK & IE Ltd.
  • Ipsen Pharma
  • Johnson & Johnson
  • Marie Stopes International
  • Meda Pharmaceuticals Limited
  • medac GmbH
  • Menarini Ricerche s.p.a
  • Merck
  • MERIAL - Comptabilité Fournisseurs
  • Monachem
  • Mylan
  • Mylan Hungary Kft
  • Nestec SA
  • OPCA Defi
  • Phara Plus Life Science Services
  • Roche
  • Shire Pharmaceuticals Development Ltd
  • Voisin Consulting
  • Zambon SpA
  • Zentiva Group a.s.

Solid content, the form was good, good speaker.

Marion Drouet, International Product Partner, Roche

Norah was clear, open for questions and sympathetic.

Vanina Premus Pogacar, Associate for Validation of Applications, Agency for Medicinal Products and Medical Devices

Overall I found this useful, some content was not so relevant, but a good general overview.

Joanna Fitch, Regulatory Affairs Senior Manager, GSK Consumer Healthcare

I got what I expected. An overview of pharmaceutical legislation, speaker was great with huge knowledge.

Danijela Jurisic, Associate for Validation of Applications, Agency for Medicinal Products and Medical Devices

Course content is very comprehensive, cannot recommend any additions. Presentation slides are also very thorough and appropriately referenced. Good speaker but could be more engaging as per previous comments

Suna Horner, Associate Medical Manager, HRA Pharma UK & IE Ltd.

Very useful course to improve the understanding of European Requirements and the different types of procedures

Tonia Mazzarella, Regulatory Affairs, Zambon SpA

The course was informative, comprehensive and interactive. The venue was fantastic and Management Forum was well organised. The entire course was well put together. Brilliant Experience!

Evelyn Olasegha, Senior Manager Regulatory Affairs, Mundipharma Research Ltd

Very useful

Carola Lempke, Senior Patent Attorney, AstraZeneca

The content is up to date, however, lack of detail explanation in each legislation and regulation (but understandably that it will be insufficient to do it in 2days course)

Chin Hooi Yeo, Gx Labelling Specialist, Zentiva Group a.s.

Nice speaker - open for discussion

Chantal Mutsaers, Regulatory Affairs Scientist, Phara Plus Life Science Services

Interesting and very valuable course.

Sofie Stalmans, Regulatory Affairs, PhaRA BVBA

Speaker was personable, knowledgeable good place and tone.

Sorwar Choudhury, Head of Medical, Pharmacovigilance and Regulatory Affairs, Meda Pharmaceuticals Limited

This kind of overall training covers a lot of topics, that's why it is very interesting

Sophie Ferruit, Scientific writer, Monachem

Overview good

Gregor Schaefer, Medical Therapeutic Area Specialist, Galderma International