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.
Hands collaborating to assemble blue puzzle pieces, symbolizing teamwork and problem-solving

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.
 
 

Related topics & resources

Patient room with white interior for clinical trials

Clinical Pharmacology Unit

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

Learn more
Doctor consulting with a patient about clinical trial recruitment

Multicentre patient studies

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

Learn more
Business people join puzzle pieces in office, concept of cinical trial supply services

Our trial solutions

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

Learn more

Frequently asked questions (FAQs)

  • Does Nuvisan offer clinical development consulting services?
    Yes, Nuvisan offers clinical development consulting services across a broad range of areas. These include advice on specific scientific and regulatory questions, preparation and review of documents required for clinical trials in humans, and support for the design and refinement of clinical trials. Nuvisan also supports the transition from the preclinical to the clinical phase, including assessment of non-clinical requirements, calculation of the maximum recommended safe starting dose and definition of dose steps in first-in-human studies. In addition, Nuvisan provides broader regulatory consulting, including support for scientific advice procedures at national and European regulatory agencies, as well as preparation of integrated clinical development plans.
  • Does Nuvisan only offer consulting services if the customer also awards the contract for conducting a clinical trial to Nuvisan?
    No. Nuvisan offers regulatory and clinical consulting as standalone services. These services can support an ongoing clinical development program, help prepare clinical trials in humans or address specific questions that arise during the regulatory approval process. Nuvisan can contribute at any stage of development. Where Nuvisan provides both consulting and trial delivery, the process may be more efficient for the customer. However, customers can choose the services that best meet their needs.
  • Are the clinical and regulatory consultants at Nuvisan qualified to do this work?
    Yes, Nuvisan’s clinical and regulatory consultants bring extensive experience in the pharmaceutical industry and the CRO sector. The team includes specialists with experience in clinical development and regulatory consulting, including board-accredited expertise in clinical pharmacology. Where specialist input is required in a particular therapeutic or scientific area, Nuvisan can also arrange advice from external clinical experts.
  • How are the consulting services billed?
    Consulting fees depend on the scope, type and duration of the work. Where consulting relates to a specific study, the cost can be included in the study budget. For standalone consulting services, Nuvisan can agree an hourly rate and an estimated range of hours in advance. Only the hours worked are billed, and time is recorded accordingly. Where a customer requires ongoing access to consulting support over a longer period, Nuvisan can also offer a retainer or service agreement.

Contact us

Nuvisan is committed to protecting your privacy, and we'll only use your personal information to administer your account and to provide the products and services you requested from us. If you consent to us contacting you for this purpose, please tick below to say how you would like us to contact you:
You can unsubscribe from these communications at any time. For more information on how to unsubscribe, our privacy practices, and how we are committed to protecting and respecting your privacy, please review our Privacy Policy.

Talk to us

talk icon
+49 731 9840 0 

Our locations

location icon

Neu-Ulm (headquarters)

Wegenerstrasse 13

89231 Neu-Ulm

Germany

Berlin

Muellerstrasse 178

13353 Berlin

Germany

Sophia Antipolis

2400 route des Colles

06410 Biot

France

Grafing

Am Feld 32

85567 Grafing

Germany

Waltrop

Im Wirrigen 25

45731 Waltrop

Germany

For concerns about pharmaceuticals or adverse drug-related events, contact us at: complaints@nuvisan.com