Where: Evenlode Boardroom, Milton Park Innovation Centre
When: 22 November 2017
Topics:
- Early-to-late phase clinical trial pharmacovigilance
- Preparation for Marketing Authorisation
- Pharmacovigilance auditing and training
- Common pharmacovigilance inspection findings and pitfalls (MHRA, BfArM)
- Need for good, efficient processes
This seminar may be useful for the following:
- - Head of Research and Development
- - Clinical Project Managers
- - Procurements / Contracts Management
- - Quality Assurance
There will also be time available after the seminar to have a complimentary one-to-one session to discuss any company specific pharmacovigilance and regulatory affairs questions (confidentiality agreements can be signed).
Please register your interest by emailing: seminars@eudrac.com
Please visit our website at www.eudrac.com