Clinical and regulatory consultancy
Founded by a team of experienced pharma professionals, with a track record of over 40 years serving clients’ needs from target identification to clinical development, Nuvisan is well positioned to support our clients with their drug development strategies all the way through to clinical phase 2. We offer:
- Advice in clinical pharmacology
- Preparing clinical trial concepts
- Writing clinical development plans (CDPs)
- Regulatory consulting, including:
- Organisation of scientific advice procedures
- Compilation of regulatory dossiers to obtain marketing authorisation approval (MAA)
- Supporting clients in the dialogue with regulatory agencies.