Individual
agenda
Flexible
location

Inhouse courses and webinars

for professionals in the drug & device industry.

We are a European based company offering training on regulatory affairs, regulatory compliance, quality assurance and business organisation in the pharmaceutical, food supplement and medical device industry.
Register for one of or current training or contact us for your individual training plan.
New! China Regulatory Affairs

China Regulatory Affairs

A series of webinars to equip your professionals with expert knowledge on the regulations for drug and device registration on the Chinese market, and on how to interact successfully with the Chinese Health Authorities.
China Regulatory Affairs
Project Management

Project Management

...for Regulatory Affairs Professionals. Ensure a smooth process and the highest quality in the pharmaceutical and medical device business.
Project management
Regulatory requirements

Regulatory requirements in the US

Equip your professionals with the basis of the regulatory requirements in the US - guidelines, legislation, variations submissions, the FDA & more.
Regulatory requirements
Labelling and packaging

Labelling and packaging in the EU

Equip your professionals with a complete technical understanding of the regulatory framework of labelling in the European Union.
Labelling and packaging