On 9 February 2026, the Scientific and Educational Center of the National Center for Expertise of Medicines and Medical Devices announced an online training seminar on pharmacovigilance.
The seminar will take place on 11 March 2026 from 10:00 to 13:00 and will be delivered by Malik Abdrakhmanov, PhD, Head of the Department of Pharmacovigilance and Monitoring of Safety, Efficiency, and Quality of Medical Devices.
The session is titled:
Modern Requirements and Regulatory Aspects in the Field of Pharmacovigilance
Seminar Overview
The training will address key pharmacovigilance and post-marketing surveillance requirements applicable in the Republic of Kazakhstan and the Eurasian Economic Union.
Topics include:
- Current international and national pharmacovigilance requirements
- The role of regulatory authorities in the pharmacovigilance system
- Responsibilities of marketing authorization holders and registration certificate holders
- Emerging trends and changes in regulatory practice
The seminar is intended for manufacturers of medicinal products, authorized representatives, applicants, and regulatory specialists seeking practical understanding of pharmacovigilance obligations within Kazakhstan and EAEU markets.
Format and Participation Details
Format: Online
Date: 11 March 2026
Time: 10:00–13:00
Participation fee: 24,857.64 tenge (including VAT)
Participants will receive a Certificate of Completion of Non-Formal Education upon completion.
Registration Procedure
To register, participants must:
- Complete and submit an individual application form in both signed PDF and Word format to [email protected]
- Conclude a training agreement with the State Enterprise on the Right of Economic Management National Center for Expertise and Medical Research under the Cabinet of Ministers and the Federal Agency for Health of the Republic of Kazakhstan
- Provide supporting documents confirming authority (state registration certificate for residents, state register extract for non-residents, and power of attorney where applicable)
- Submit the draft agreement to [email protected] for legal review
- Deliver two signed hard copies of the agreement to 63 Ablai Khan Ave., Office 304, Almaty
- Submit the mandatory “Payment Application” appendix in signed PDF and Word format
- Complete payment upon receipt of the invoice and send confirmation before the training date
Regulatory Context
This seminar supports continued professional development in pharmacovigilance and aligns with increasing regulatory scrutiny across Kazakhstan and the EAEU region. As regulatory frameworks evolve, structured pharmacovigilance systems, compliance monitoring, and lifecycle safety management remain essential for marketing authorization holders operating in Eurasian markets.
For more information: On holding a training seminar on pharmacovigilance issues
