FDA and MHRA Pharmacovigilance Inspection Readiness and Management

This discussion is geared for the pharmaceutical industry. It will provide pharmacovigilance (product safety) departments with solid ideas to help them prepare for and manage a health authority inspection. Medical information, research and development and quality and compliance groups in the pharmaceutical industry would benefit from tips discussed in this session as well.

Why Should You Attend:

This webinar is for anyone working in a regulated environment such as pharmacovigilance, medical information, quality and compliance or research and development. There is a very good chance that you will be inspected by a health authority, maybe you have been inspected already and you are anticipating their return. 

Who Will Benefit:

Pharmacovigilance/ product safety departments

Medical information groups

Research and development groups in the pharmaceutical industry

Quality and compliance groups in the pharmaceutical industry

Instructor Profile:

Dr. Kathleen Humel holds a doctor of pharmacy degree and is a licensed pharmacist. She worked as a retail pharmacist, pharmacy manager and trainer for eight years for independent as well as chain pharmacies. She ventured into the pharmaceutical industry and has remained there for 14 years. Dr. Humel worked as a drug safety associate and gradually worked her way up to a management position, overseeing a pharmacovigilance document management group for several years.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/fda-and-mhra-pharmacovigilance-inspection-readiness-and-management-webinar-training-704181-prdw?channel=sciencedz