Grzegorz Cessak

President at The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products

Grzegorz Cessak

Grzegorz Cessak

President at The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products

Overview
Career Highlights

The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products

RelSci Relationships

521

Number of Boards

1

Relationships
RelSci Relationships are individuals Grzegorz Cessak likely has professional access to. A relationship does not necessarily indicate a personal connection.

Professor of Microbiology at The American University of Rome

Relationship likelihood: Strong

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

Relationship likelihood: Strong

Head, Public Engagement Department at The European Medicines Agency

Relationship likelihood: Strong

Executive Director at Slovakia State Institute for Drug Control

Relationship likelihood: Strong

President at The Federal Institute for Drugs & Medical Devices

Relationship likelihood: Strong

Director, Post-Licensing at Malta Medicines Authority

Relationship likelihood: Strong

General Director at European Brain Research Institute(EBRI)

Relationship likelihood: Strong

Editor at Der Arzneimittelbrief

Relationship likelihood: Strong

Former Chief Executive Officer at Medicines & Healthcare Products Regulatory Agency

Relationship likelihood: Strong

Head of Austrian Medicines & Medical Devices Agency at Austrian Medicines and Medical Devices Agency

Relationship likelihood: Average

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Grzegorz Cessak
President at The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products
Education
Master Degree in Pharmacy
Class of 2001

Medical University of Warsaw is a school in Warsaw.

Career History
Vice Chair, Management Board
Prior - 2019

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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