BREXIT What's Changing for Life Science Product License Holders/Manufacturers and What You Need to Do Right Now?

Robert J. Russell

Starting at

$349


Buy Now

This webinar will discuss how to accurately assess the impact of Brexit up on your operations and existing licensed life products in the UK and EU. How to plan to becoming compliant on “what is known” and how to be agile as the rest of implications become clearer. Impact on Filing Registrations with EMA in Q1 2019, How Will the UK’s Withdrawal Effect the Sunset Clause.

Why Should You Attend:

The United Kingdom submitted its’ notification on 29 March 2017 to withdraw from the European Union. This means that unless a withdrawal agreement establishes another date, all EU primary and secondary Laws cease to apply to the UK from 30 March 2019 going forward. The UK, by definition would become a “third country”. Preparing for the withdrawal doesn’t just involve the Healthcare Authorities, but every manufacturer and / or license holder of a pharmaceutical, biologic, medical device or combination product in the UK and EU.

Marketing Authorization holders of centrally authorized or mutually authorized [MRP / DCP] product licenses for pharmaceuticals and biologics along with CE-marked medical devices for human or veterinary use will have legal repercussions when the UK exits the EU. While there is still considerable uncertainty in a withdrawal agreement, there is now enough known about the likely implications that manufacturers and license holders need to start making plans NOW, so they don’t find themselves in Non-Compliance with the new legal framework.

Attend this webinar to understand how to accurately determine how Brexit will affect the operations and existing licensed Life Science Products in the UK and EU. It will allow companies to make plans on becoming compliant on “What is Known” and to remain agile as the rest of the implications become clearer.

Learning Objectives:

Upon completion of this course, attendees will be able to accurately determine how Brexit will affect their operations and existing licensed Life Science Products in the UK and EU. It will allow companies to make plans on becoming compliant on “What is Known” and to remain agile as the rest of the implications become clearer.

Detailed Agenda of the Session:

  • EU Regulatory and Legislative Structure [with and without the UK]
  • Issued Laws: Directives vs. Regulations
  • Impact on Filing Registrations with EMA in Q1 2019
  • Brexit Impact on License Holders Established in the UK
  • What if my EU Authorized Representative is Located in the UK?
  • What if the QPPV Resides in the UK?
  • What if API Manufacturing is Located in the UK?
  • What if Finished Product Manufacturing is Located in the UK?
  • What if Batch Release is Done in the UK?
  • What’s the Effect on Generic or Hybrid Licenses Against a Reference Product Authorized in the UK?
  • What’s the Effect on More Specialized Products Like Herbal Medicines or Orphan Drugs?
  • How Will the UK’s Withdrawal Effect the Sunset Clause?
  • What’s the Effect Difference on Nationa or Mutual Recognition [MRP / DCP] Licenses vs. Centrally-Licensed Products?
  • How is Brexit anticipated to Effect CE Certification or ISO-13485 Certification on Medical Devices?
  • Wrap-Up and Q&A

Who Will Benefit:

This workshop will be of great value to companies manufacturing in the UK / EU or holding Marketing Authorizations in the UK / EU. It is primarily designed to benefit personnel within the following disciplines:

  • Executive & General Management
  • Legal
  • Regulatory Affairs
  • Quality Assurance
  • Manufacturing / Distribution
  • Clinical Research
  • Product Development
  • CROs
  • Consultants
Webinar Events
Live -Coming soon!

Training CD-DVD

Physical CD-DVD of recorded session will be despatched after 72 hrs on completion of payment


Recorded video

Recorded video session



Speaker: Robert J. Russell,

Robert J. Russell, (Bob) is the President of RJR Consulting, Inc. RJR Consulting Inc. specializes in understanding global regulatory issues for the pharmaceutical industry. Bob has more than 25 years of experience working with FDA and the Commission on technical issues as they relate to policy development, regulation, clinical trial and the medical device development process. Prior to entering the consulting field, Mr. Russell was the Global Director of Regulatory Affairs for two Fortune 100 firms. These companies were major raw material suppliers to the pharmaceutical and medical device industry and one a joint-venture parent of a major pharmaceutical division.


Follow us

Toll Free

1-866-978-0800

Fax

1-888-883-7697