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IND/NDA enabling services

Accelerate your path to approval

Nuvisan's CMC experts streamline drug development timelines, from synthesis route design t GMP/non-GMP material production. Our formulation specialists create innovative, scalable solutions tailored to your needs, while our three GMP sites provide analytical excellence. With tailored documentation, professional project management and IND-focused support, we help accelerate regulatory submissions.

Illustrates a scenario that highlights how advanced document management technologies ensure regulatory compliance and governance standard

Ideal partner for NDA/IND preparation

Our chemistry experts based in France will develop the best synthesis route for the successful manufacture of your GMP and non-GMP materials required for clinical and non-clinical studies.

With three GMP sites, Nuvisan CMC offers comprehensive analytical support to help ensure the quality of your active substances and drugs. With professional project management to monitor the progress of your project, Nuvisan is the ideal partner for integrated services in support of IND preparation. 

With the full range of CMC services offered by Nuvisan, we can generate the tailored documentation needed to support the scientific writing of your dossier (specifications, methods, reports and CoA) and for all products.

 
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