Master-class
Watch the programMaster-class
Opening of Master-class “Technology Transfer. Regulatory Requirements”
Moderator

Yelena Denisova
Deputy Director of the Department of Pharmaceutical and Medical Industry Development, Ministry of Industry and Trade of the Russian Federation

Natalia Chadova
Head of Pharmaceutical Production Inspection and Expertise Department of FSI “SID&GP”, Russian Ministry of Industry and Trade

Ekaterina Nikifirova
Deputy Head of the Department for Drugs Inspection and Expertise, “SID & GP” of the Russian Ministry of Industry and Trade
Participants
Natalia Burlakina
Leading Specialist of the Section for Drug Manufacturing Sites. “SID & GP” of the Russian Ministry of Industry and Trade

Ferenc Lukács
Inspectorate Head of National Institute of Pharmacy and Nutrition (OGYÉI), Hungary
Lisette Pérez Ojeda
Advisor to CECMED´s Director
Suzana Jukić
Senior GMP Inspector of Agency for Medicinal Products and Medical Devices of Croatia (HALMED)

Patricia Aprea
Director of Evaluation and Control of Biologicals and Radiopharmaceuticals), National Administration of Drugs, Foods and Medical Devices (ANMAT) /National Institution of Drugs (INAME)

Vera Korobova
Head of Group for Introducing New Products, Gedeon Richter
Timur Nazarov
Chief technologist, Mechnikov Scientific Research Institute of Vaccines and Serums
Mikhail Meshalkin
Senior Specialist of the Support Group for Manufacturing and Transfer, Takeda

Nguyen Ly
Executive Director, Biologics Technical Product Leadership, MSD Pharmaceuticals
Marina Mishustina
Project manager, Novo Nordisk
Tina Norup
Project manager, Novo Nordisk

Olga Maklakova
Corporate Quality Director, Binnopharm