Speaker Profile

Adriaan Fruijtier
Adriaan Fruijtier
Regulatory Affairs Consultant , CATS Consultants GmbH,

Adriaan Fruijtierhas graduated as a pharmacist at the University of Utrecht, The Netherlands.

He is currently Director Regulatory Affairs at CATS Consultants. Until March 2004 he has been Head of the Oncology Group within Global Regulatory Affairs at Bayer AG, Wuppertal, Germany, and Bayer Corporation, West Haven, CT, USA. Between 2001 and 2003 he was Director of Regulatory Affairs at Micromet AG, a biotech company in Munich, Germany. Prior to joining Micromet he has worked during four years as a Project Manager for Oncology Projects at the European Medicines Agency in London, United Kingdom

He joined the European Medicines Agency from Novartis AG, Basel, Switzerland, where he was Regulatory Affairs Project Manager in the Oncology group in 1996 and 1997. Before 1996 he was Head of Drug Regulatory Affairs for six years at Ciba-Geigy in the Netherlands, and has worked as Manager Regulatory Affairs at Glaxo, also in the Netherlands.

Upcoming Webinars Recorded Webinars
  • 24
  • June
  • 2021
  • Thursday
08:00 AM PDT | 11:00 AM EDT

6-Hour Virtual Seminar on EU Regulatory Affairs Strategy During Development of Medicinal Products

The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan.

Adriaan Fruijtier Adriaan Fruijtier | Duration:6 Hours | Price: $545.00 | View Details
Adriaan Fruijtier

6-Hour Virtual Seminar on EU Regulatory Affairs strategy during development of medicinal products

The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan. In this Seminar it is explained how to write the regulatory plan, and which aspects to consider.

Speaker: Adriaan Fruijtier | View Anytime | Duration: 6 Hours | Price: $595.00 | View Details
Adriaan Fruijtier

6-Hour Virtual Seminar on EU Regulatory Affairs Strategy During Development of Medicinal Products

The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan.

Speaker: Adriaan Fruijtier | View Anytime | Duration: 6 Hours | Price: $595.00 | View Details
Adriaan Fruijtier

6-Hour Virtual Seminar on EU Regulatory Affairs strategy during development of medicinal products

The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan. In this Seminar it is explained how to write the regulatory plan, and which aspects to consider.

Speaker: Adriaan Fruijtier | View Anytime | Duration: 6 Hours | Price: $945.00 | View Details
Adriaan Fruijtier

6-Hour Virtual Seminar on EU Regulatory Affairs Strategy During Development of Medicinal Products

The main document from a regulatory perspective in the development of a medicinal product is the regulatory plan.

Speaker: Adriaan Fruijtier | View Anytime | Duration: 6 Hours | Price: $945.00 | View Details