Jean-Claude Rouby

Chair, Ad Hoc Group on Novel Veterinary Therapies, Committee for Medicinal Products for Veterinary Use at The European Medicines Agency

Jean-Claude Rouby

Jean-Claude Rouby

Chair, Ad Hoc Group on Novel Veterinary Therapies, Committee for Medicinal Products for Veterinary Use at The European Medicines Agency

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RelSci Relationships

485

Number of Boards

1

Relationships
RelSci Relationships are individuals Jean-Claude Rouby likely has professional access to. A relationship does not necessarily indicate a personal connection.

Head of Working Parties Secretariat (Ad Interim) at The European Medicines Agency

Relationship likelihood: Strong

Head, Public Engagement Department at The European Medicines Agency

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Head of Labelling Review & Standards Office at The European Medicines Agency

Relationship likelihood: Strong

Member, Committee for Advanced Therapies at The European Medicines Agency

Relationship likelihood: Strong

Member, Committee on Herbal Medicinal Products at The European Medicines Agency

Relationship likelihood: Strong

Member, Committee for Advanced Therapies at The European Medicines Agency

Relationship likelihood: Strong

Member, Paediatric Committee at The European Medicines Agency

Relationship likelihood: Strong

Member, Committee for Medicinal Products for Veterinary Use at The European Medicines Agency

Relationship likelihood: Strong

Member, Committee for Medicinal Products for Veterinary Use at The European Medicines Agency

Relationship likelihood: Strong

Member, Pharmacovigilance Risk Assessment Committee at The European Medicines Agency

Relationship likelihood: Strong

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Jean-Claude Rouby
Chair, Ad Hoc Group on Novel Veterinary Therapies, Committee for Medicinal Products for Veterinary Use at The European Medicines Agency
Boards & Committees
Chair, Ad Hoc Group on Novel Veterinary Therapies, Committee for Medicinal Products for Veterinary Use
2015 - Current

The European Medicines Agency is a decentralised agency of the European Union, located in London. The Agency is responsible for the scientific evaluation of medicines developed by pharmaceutical companies for use in the European Union.

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