Clinical development
With several years in leading clinical trials and have been here through many evolutions of the industry. Along with Sponsors and CROs, P.H.C & S has learned how to ensure safety for study subjects, execute protocols precisely, speed-up start-up activities (selection/qualification of sites, collection of essential documents, contract negotiation...), enhance the recruitment, maximize subject retention, collect reliable data and provide reliable and responsive communication of study data throughout.
P.H.C & S helping you in the development of the blueprint of a drug/medical devices entire clinical research strategy, mapping potential partners. It outlines the clinical program design, including development, assessment, decision points, personnel, and budgetary estimates.
P.H.C & S working with a partner with strong Digital Platform Technology for Life Science.
Helping you to determine the safety and efficacy of medications and treatments intended for human use.
If necessary, lead teams and manage operational aspects throughout the clinical trial and facilitate the development of clinical documents.
The ultimate goal of clinical development is to obtain the clinical information that will be included on the labelling of the new medicine.
Would you like more information?
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