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This content is a press release from our partner Business Wire. The AP newsroom and editorial departments were not involved in its creation.

Two Day Course: Pharmaceutical Development of ATMPs - London, United Kingdom - April 4th-5th, 2019 - ResearchAndMarkets.com

March 6, 2019

DUBLIN--(BUSINESS WIRE)--Mar 6, 2019--The “Pharmaceutical Development of ATMPs” conference has been added to ResearchAndMarkets.com’s offering.

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.

The programme will cover the regulatory landscape, the definition and classification of ATMPs and provide practical guidance on how to overcome quality and specific GMP challenges. Comparison of the differences between GMP for Advance Medicinal Therapeutic Product (ATMPs) and conventional therapeutics will be discussed. Consideration of what is required for clinical trials and the preparation of the IMPD will also be addressed. Furthermore advice on the specific transportation requirements of these products will be included.

This programme will be of benefit to all those involved with or considering developing an AMTP.

Benefits of attending:

  • Understand the GMP requirements at Phase 1 in US and Europe
  • Gain a practical insight into other markets
  • Determine critical quality attributes
  • Develop a successful QC strategy
  • Examine the major differences between GMP for ATMPs and conventional therapies
  • Overcome potential pitfalls when manufacturing cells
  • Discuss multi manufacturing sites for autologous products
  • Consider stability issues
  • Examine risk analysis for biological materials
  • Gain an introduction to GMO approval requirements

Who Should Attend:

  • R & D personnel involved in research on cell or gene based therapies
  • Managers involved in the development and manufacture of ATMPs
  • Quality assurance and quality control personnel responsible for quality aspects of ATMPs
  • GMP managers responsible for implementing GMP in ATMP manufacture
  • Regulatory personnel involved in inspections of ATMPs

Agenda:

Day one

Introduction to ATMPS

  • Definition of ATMPs and associated terms
  • Classification of ATMPs

The regulatory landscape

  • Examining the European regulatory landscape for ATMPs - detailed analysis of existing regulation 1394/2007
  • Considering factors lying outside of the regulation’s scope, e.g. combination products
  • Links to related directives, eg Tissues and Cells Directives (2002/98/EC and 2004/23/EC); Medical Devices Directive (93/42/EEC) and forthcoming regulation

Understanding clinical trials

  • EU clinical trial requirements
  • The US IND

Strategic considerations

  • Opportunities to meet with regulators to maximise approval chances
  • ATMP-specific options in the EU: certification procedure, risk-benefit approach
  • Accelerated access opportunities in EU and US
  • Understanding breakthrough status/PRIME

Insight into global regulations and requirements

  • Examining key markets including Europe, US and Japan
  • Evaluate the regulatory differences between regions to help you build a strategic approval route
  • GMP requirements at Phase I in US and Europe - ramifications for your product

Overcoming quality challenges

  • Overview of frequent quality concerns
  • Potency assay development
  • Determining critical quality attributes
  • Developing a successful QC strategy for short shelf-life product
  • QP release: timing and logistical challenges for ATMPs

Risk-based approach for ATMPs

  • Examining 3.2.A Adventitious Agents
  • Level of data required EU/US

Programme Day Two

GMP for ATMPs

  • What is required: examine the major differences between GMP for ATMPs and conventional therapeutics
  • Overcoming potential pitfalls when manufacturing cells
  • Current GMP interpretations
  • Multiple manufacturing sites for autologous products
  • Point-of-care preparation devices

Delivery and shipping

  • Considering stability issues
  • Challenges in transporting cell therapies/cryopreservation
  • Preparation on site

Preparation for clinical trial

  • Optimising materials for regulatory compliance - vendor qualification
  • Risk analysis for biological materials
  • The comparability concept and its importance in preparing for clinical trials
  • Introduction to GMO approval requirements

Practical considerations for the Investigational Medicinal Product Dossier (IMPD)

  • Terms and definitions
  • Guidance on IMPD content for ATMPs
  • Data requirements for first-in-human vs later clinical trials

For more information about this conference visit https://www.researchandmarkets.com/research/r3fzrj/two_day_course?w=4

View source version on businesswire.com:https://www.businesswire.com/news/home/20190306005426/en/

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Related Topics:Drug Discovery

KEYWORD: UNITED KINGDOM EUROPE

INDUSTRY KEYWORD: HEALTH PHARMACEUTICAL

SOURCE: Research and Markets

Copyright Business Wire 2019.

PUB: 03/06/2019 08:39 AM/DISC: 03/06/2019 08:39 AM

http://www.businesswire.com/news/home/20190306005426/en