Learn all you need to know to communicate effectively with toxicologists

This three-day course will help you understand the European regulatory requirements for developing labelling and package leaflets and clearly interpret the Directive 92/27/EEC. The course will also provide practical guidelines and advice on designing and writing SPC and Patient Information Leaflets that meet regulatory requirements and satisfy readability and compliance needs.

In the face of increasing regulatory and consumer demand, the need for accurate and complete product information has never been stronger. This course will provide you with key practical information on devising successful labelling strategies to guarantee you get it right first time.

Who Will Attend?
This course has been specifically designed to address the training needs of Managers and Executives in area such as
> Regulatory Affairs
> Product Labelling
> Legal Counsel
> Drug Safety
> Medical Affairs
> Marketing
> Medical Information

The course will be beneficial to people new in their role, and more experienced professionals who need clarification on the new requirements.

Course Leader
Axel F. Wenzel (PhD, MSc, MBira) is the Managing Director of p.ss.t Pharma Scientific Services Team Ltd, a service and consulting company for drug and medical device development. Hoss A. Dowlat, PhD is a Senior Regulatory Consultant at Parexel International Corporation. He is a science-based regulatory affairs manager and a strategic thinker with 22 years experience in North American and European pharmaceutical industry.

Registration required:

Yes

Free:

No