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VCLS senior consultants regularly share practical considerations about developing
health products more effectively. International conferences and VCLS series of
workshops provide meeting opportunities on both sides of the Atlantic.

Building quality documentation early during development

Florence Philippoz will be the moderator of a session entitled “Building quality documentation early during development” for the SME Workshop “Focus on Quality for Medicines containing Chemical Entities” hosted by the European Medicines Agency, on April, 4, 2014 in London, UK.

This session will overview the applications for marketing authorization, the quality aspects in investigational medicinal product development, the GMP issues for start-ups, quality in the supply chain and role of QP.

Contact us if you would like to meet Florence.

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Anticipated Upcoming Changes in European MedTech Regulation

Anticipated Upcoming Changes in European MedTech Regulation: Business impact and practical considerations

March 24th, 2014 – 11:30am-1:30pm

Massachusetts Biotechnology Council, Cambridge, MA

Voisin Consulting Life Sciences organizes another of a series of discussions on how the European regulatory scene will evolve in 2014, and what impact it will have for manufacturers.

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