Anna Harrington-Morozova

Anna Harrington-Morozova is a regulatory, drug development and external relations professional with over 20 years’ experience gained working in a Regulatory Authority, academia and industry. Anna graduated in Russia as a pharmacist. After working in the Russian Ministry of Health and the Clinical Pharmacology Department of Moscow Medical University, she held regulatory and external relation positions in the pharmaceutical industry and CROs in Russia and the UK, including senior regulatory affairs posts in GSK,EISAI, ICON and PRA. Anna currently acts a a Scientific and Reguatory director at Regem Consulting Ltd – a consultancy which focuses on drug development, global regulatory advice, professional trainings and flexible resourcing solutions for the pharmaceutical, biotech and medical device industries in emerging markets.

Training format

Topic

  • Next: 6-7 Feb 2025 Live online
  • Also: 19-20 Jun 2025 Live online
  • Also: 2-3 Oct 2025 Live online

Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union

Live online

This interactive course will discuss the regulatory requirements for human pharmaceuticals within these regions, and discuss the implications of the new joint Eurasian Union regulation.

  • 12 CPD hours Focused
  • Presented by Anna Harrington-Morozova
  • Next: 3-4 Apr 2025 Live online
  • Also: 23-24 Jul 2025 Live online
  • Also: 8-9 Dec 2025 Live online

Medical Device Regulation in the Eurasian Union, Russia and the CIS

Live online

A comprehensive overview of medical device regulatory affairs in Russia and the Eurasian Union. Key countries covered include Armenia, Azerbaijan, Belarus, Georgia, Kazakhstan, Kyrgyzstan, Moldova, Russia, Tajikistan, Turkmenistan and Ukraine.

  • 12 CPD hours Focused
  • Presented by Anna Harrington-Morozova