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Market research for the future of the medicinal product or medical device.

 

Determination of regulatory requirements in line with current directives and guidelines.

 

Selection of necessary non-clinical and clinical trials and strategic planning for these studies.

 

Preparation of product development timelines indicating critical path, milestones and resources needed.

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Our services

Translation

Data Management

Clinical Trials

Medical Writing

Product Registration

Observational studies

Pre-clinical Studies