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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.

Increase commercial value through an integrated EU and US regulatory strategy

June 9, 2014 – 5pm -7:30pm
Royal College of Surgeons 35-43 Lincoln’s Inn Fields, London, WC2 3PE

Voisin Consulting Life Sciences and Regulatory Resources Group (RRG) organize another series of discussions on valuables insights on how to increase commercial value through an integrated EU and US regulatory strategy.

Seminar Topics will include integrating FDA into drug development programs early to support faster approvals. FDA regulatory opportunities for speeding products approval:

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MEDTEC Europe Conference

Mr. Christophe Amiel, Director, Medical Devices will be a Panelist at MEDTEC Europe Conference which will be held in Stuttgart, Germany on the 3 - 5 June 2014 at the Messe Stuttgart Convention Centre.

Christophe will be the panelist for a workshop titled, “Clinical data requirements for Combination products: what the proposed EU legislative revisions will change”. He will also discuss the current trends and key drivers in drug/device combinations market.

Contact us if you would like us to arrange for a meeting with Christophe.

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Meet with Dr. Emmanuelle M. Voisin in Shanghai

Meet with Dr. Emmanuelle M. Voisin in Shanghai, China

Emmanuelle will be participating in the 16th Shanghai International Forum on Biotechnology & Pharmaceutical Industry (May 22-24, 2014), where she will take part in several panel discussions. Dr. Voisin will also speak of how to seek feedback from regulators and payers on clinical development, to ensure successful approval and commercialization in both Europe and the US.

Contact us to arrange for a meeting with Emmanuelle.

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Clinical Development Plan: Obtain Insights from Regulators and Payers

Clinical Development Plan: Obtain Insights from Regulators and Payers

May 8th, 2014 – 11:30am-1:30pm

Massachusetts Biotechnology Council, Cambridge, MA

Voisin Consulting Life Sciences organizes another series of discussions on how to couple regulators’ scientific advice with payers’ opinion prior to Phase 3 to ensure successful approval and commercialization in both Europe and the US.

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