Clinical development consulting

Strategic support

Our experienced professionals understand that the modern healthcare industry requires customised strategies to rapidly and efficiently advance compounds to the next phase while helping ensure the highest quality. Nuvisan has a track record of providing expert consulting to satisfied clients in various areas of drug development.
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Consulting for clinical trial design

Nuvisan can assist in your product development by creating a clinical study protocol (CSP) design to meet the regulatory objectives regarding primary and secondary endpoints for your investigational medicinal product (IMP). Nuvisan can further assist clients with the set-up of a clinical development plan (CDP) detailing required clinical phases, study designs and regulatory requirements.
Strategic decision making for clinical trials and clinical development programs

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.
 
 

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Clinical Pharmacology Unit

Our clinical pharmacology unit conducts early phase clinical trials for our clients for over 40 years.

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Doctor consulting with a patient about clinical trial recruitment

Multicentre patient studies

We provide clinical development support for your multicentre phase 1-2 trials.

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Our trial solutions

Discover how our comprehensive clinical trial services can support your efforts.

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