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Heathics Paris France, pharmaceutical industry consultant, pharmaceutical laboratory consultant team,  study, trial, consultant, paediatric investigational plan, registration files ctd,

Heathics Paris France, pharmaceutical industry consultant, pharmaceutical laboratory consultant team,  study, trial, consultant, paediatric investigational plan, registration files ctd,
Heathics Paris France, pharmaceutical industry consultant, pharmaceutical laboratory consultant team,  study, trial, consultant, paediatric investigational plan, registration files ctd,
  pharmaceutical industry consulting in France, pharmaceutical laboratory consulting, drug safety, clinical study, medical market consultants, scientific communication consulting,
 





Heathics health pharmaceutical industry consultant

health pharmaceutical industry consultant

Heathics partners

Values health pharmaceutical industry consultant


Heathics Paris France, pharmaceutical industry consultant, pharmaceutical laboratory consultant team,  study, trial, consultant, paediatric investigational plan, registration files ctd,


Vidal Benatar

Vidal Benatar


Vidal Benatar graduated from the Medical School of Paris, France. After 10 years of clinical practice in Internal Medicine, he joined the Pharmaceutical Industry where he acquired a 25-year experience in Research and Development and Medical Affairs in large global companies, leading the development and European registration of innovative medicines for Cardiovascular, Respiratory and Bone diseases.

Vidal Benatar has gained extensive experience in international Phase I to Phase III drug development, registration and pricing. This experience includes generation and oversight of clinical development strategies, completion of multiple large international trials, development of CTDs and other registration files, and interactions with European Regulatory Agencies (especially the EMEA) as well as the FDA.

Patricia Nury

Patricia Nury


Patricia Nury graduated from the Medical School of Paris, France. After 5 years of clinical practice in Internal Medicine and Geriatrics, she joined the Pharmaceutical Industry where she acquired nearly 20-year experience in New Drug Development with focus on Clinical Research, Global Project Management and Regulatory Strategy for Cardiovascular and Central Nervous System medicines.

As a Global Drug Development Project Director, Patricia Nury has taken responsibility for clinical development plans, designing phase II, III and IV protocols, global program management (including supervision of data-management, biostatistics and medical writing) and the technical component of the regulatory strategy. In this role, she oversaw a large group of clinical researchers. She also participated actively in the overall risk management plan and post-approval pharmaco-epidemiological studies. Ultimately, she was highly involved in registrations to the EMEA, Australia, and Canada and led the development of registration plans for Japan, China, and Taiwan.








Heathics
111, rue des Tennerolles - 92210 Saint Cloud, France
Phone/Fax : 33+ (0)1 46 02 19 30.


Links


Conception - réalisation
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