Do you need a professional service for your pharmaceutical products that provides rapid and personalised responses to your needs? Regulatory Affairs Consultancy is there for you: from the moment you have an idea for a product all the way to the “final” variation, we provide you with operational support in all phases of medicinal product authorisation especially in Europe.
What distinguishes us
Extensive years of experience and a professional, diligent, well-organized and team-oriented performance
From the first pilot batch to clinical trials and all the way to submission for authorisation: we put your ideas into operation.
How we convince
A national and international network of renowned experts from the fields of human medicinal products and Medical devices are on site and at your disposal.