How is the Implementation of FMD Going - Successes and Challenges

About this course

Time: 10am EST - Duration: 1 hr

This webinar is designed to provide an update on the European Falsified Medicines Directive including guidelines on API importation, excipient GMP risk assessments, supply chain controls and safety features (tamper evidence and track-and-trace). This will include an update on the phased implementation timeline and how companies are responding.

What You Will Learn

• Latest information on the European Falsified Medicines Directive
• Implications for pharmaceutical, biopharmaceutical and generic manufacturers, brokers and distributors
• What you can do to help your company be prepared and reduce the risk of supply disruption

Course outline

• Latest information on the European Falsified Medicines Directive
• Implications for pharmaceutical, biopharmaceutical and generic manufacturers, brokers and distributors
• What you can do to help your company be prepared and reduce the risk of supply disruption

Venue

Webinar

Please register through the ‘book now’ button on the right to receive joining instructions

Tutors

We believe that our team of experts are the best available. Not only have they got years of experience in the industry, but they are committed to tutoring and helping those inside the industry to improve and raise the standards. We understand that you attend courses to learn about the latest regulations and to get your questions answered.

Our expert for this webinar is:

• 

  Mr Peter Gough
  Executive Director
  MSc, CSci, CChem, FRSC, FCQI, CQP

  • [email protected]
  • +44(0)1751 432999

What you've said

This is a new webinar for 2014 - Feedback from the delegates to follow after the course takes place.