R&D Consultancy

Our daily experience with all aspects of clinical research and drug registration has thoroughly familiarized us with international regulatory authorities´ requirements pertaining to quality and to preclinical and clinical studies. We offer early R&D consultancy to prevent our clients from making expensive detours or running into dead ends in pharmaceutical development. This is why our clients - especially those of long standing - will involve us early on in their planning.

You will receive from us:

• Development concepts
• Interface management between quality, preclinical and clinical studies
• Master plans
• Project management
• Meetings with registration authorities to coordinate further proceedings