News – State Expert Center of the Ministry of Health of Ukraine

Organization of clinical trials in healthcare facilities: the Center hosted a BPR seminar for industry specialists

18.06.2026 278

The Center held a webinar with CPD points on organizing clinical trial sites in healthcare facilities. The event brought together investigators,…

A seminar on the registration of generic and hybrid medicinal products was held at the Center

17.06.2026 284

The Center hosted a workshop “All about generics and hybrids. What is similar and what is different. Requirements for demonstrating properties”, organized…

HTA training for medical devices was held at the Center

04.06.2026 317

Recently the first seminar took place, devoted to expanding the scope of health technology assessment (HTA), namely the introduction of HTA for medical devices…

How the external reference price of a medicinal product is formed: the Center held a training webinar

28.05.2026 335

A webinar on pricing tools for medicinal products was held at the State Expert Center of the Ministry of Health of Ukraine. The training is aimed at raising awareness among applicants…

Participants of the Center's seminar discussed new regulatory approaches to documents accompanying a medicinal product

25.05.2026 423

A workshop “Documents accompanying a medicinal product: summary of product characteristics, package leaflet, labeling of the medicinal product packaging….” was held at the State Expert Center of the Ministry of Health of Ukraine.

The Center held a seminar on preparing for a clinical audit of a clinical trial

19.05.2026 344

Clinical audit is an important component of ensuring the quality of clinical trials. It makes it possible to assess compliance with the requirements of Good Clinical Practice (GCP), the organization…

A seminar-training “HTA – a tool for assessing the value of medical technologies in terms of the cost-effectiveness analysis of medical technologies” was held at the Center

15.05.2026 305

How can we assess not only the effectiveness of a medical technology but also its value for the healthcare system and the patient? This is exactly what…

Medicinal product risk management: the Center held a seminar for applicants on the specifics of developing and updating RMPs

21.04.2026 468

The Risk Management Plan is a key document of each applicant's pharmacovigilance system. It is part of the registration dossier and defines the safety profile of the medicinal…

A workshop on practical aspects of pharmacovigilance took place

01.04.2026 504

After receiving the registration certificate, the product enters the market, and the applicant's responsibility grows. Why pharmacovigilance is not just a legal obligation…

Improving research quality and patient safety – Good Clinical Practice training

27.03.2026 508

Today the Center held online training on Good Clinical Practice. The goal is to give participants a clear understanding of the regulatory requirements for the preparation and…

Organization of clinical trials in healthcare facilities: the Center hosted a BPR seminar for industry specialists

A seminar on the registration of generic and hybrid medicinal products was held at the Center

HTA training for medical devices was held at the Center

How the external reference price of a medicinal product is formed: the Center held a training webinar

Participants of the Center's seminar discussed new regulatory approaches to documents accompanying a medicinal product

The Center held a seminar on preparing for a clinical audit of a clinical trial

A seminar-training “HTA – a tool for assessing the value of medical technologies in terms of the cost-effectiveness analysis of medical technologies” was held at the Center

Medicinal product risk management: the Center held a seminar for applicants on the specifics of developing and updating RMPs

A workshop on practical aspects of pharmacovigilance took place

Improving research quality and patient safety – Good Clinical Practice training

Forum "PHARMEXPERT 2026: pharmaceutical market in the new regulatory reality"

Forum "Clinical and preclinical studies in wartime: organization and development prospects"

Pharmaceutical forum "PHARMEXPERT 2025. eCTD and pricing in Ukraine – a strategic path to integration into the international regulatory space"

PHARMEXPERT 2024. Standards. Innovations. European integration