Announcements of training events

(Enrollment closed). On 25 September 2026 we invite you to an online seminar on Good Clinical Practice (GCP): what ICH E6(R3) changes for clinical trials

07.08.2026 675

(Enrollment for this date is closed. Follow the announcements). 25 September 2026 – certified online seminar "Good Clinical Practice (GCP). Regulatory…

On 31 July 2026, we invite you to the practical seminar “The Most Common Non-conformities Identified During Audits of Applicants’ Pharmacovigilance Systems. Development of a Corrective and Preventive Action Plan”

16.06.2026 518

The purpose of the training is to provide up-to-date information on typical non-compliances identified during audits of applicants’ pharmacovigilance systems, to familiarize with practical…

On 8 July 2026, we invite you to the online seminar “The Applicant’s Pharmacovigilance System. Current Requirements and Expected Changes”

12.06.2026 726

The purpose of the seminar is to build a systematic understanding of the specifics of submitting safety reports, approaches to medicinal product safety strategy, and measures for…

19 June – certified online seminar “Good Clinical Practice (GCP). Regulatory framework for conducting clinical trials”

05.06.2026 1106

The purpose of the seminar is to deepen understanding of the updated principles and mandatory provisions of Good Clinical Practice (GCP) and the current legal regulation of clinical trials…

On June 10, 2026 we invite you to the workshop “Everything about generics and hybrids. What is similar and what is different. Requirements for demonstrating properties”. We look forward to your applications!

03.06.2026 1418

The purpose of the seminar is to give participants a systematic understanding of the requirements for demonstrating bioequivalence; planning, conducting and evaluating comparative pharmacokinetic studies, as well as…

On 17 June 2026, we invite you to the seminar-training “HTA – a tool for assessing the value of medical technologies in terms of analysis of comparative clinical effectiveness and safety.” For the first time – in online and offline formats!

02.06.2026 741

The training is aimed at developing practical skills in preparing dossiers for state health technology assessment (HTA) in accordance with the provisions of the Guideline on…

16 June 2026 – professional development seminar “The role of clinical trials in the development of medicinal products”, +3 points to the professional portfolio

29.05.2026 554

Clinical trials are one of the key stages in the development of medicinal products. It is clinical studies that confirm the efficacy, safety and…

23 June 2026 – workshop “Methodology for developing and implementing standards of medical and rehabilitation care”

28.05.2026 366

We invite doctors and other medical professionals, heads of healthcare facilities to a seminar on the methodology of development and implementation of standards of medical…

09 June 2026 – CPD seminar “Organization of the trial site in a healthcare facility”, 3 points to the portfolio

15.05.2026 550

We invite health care workers to take part in a CPD seminar on the organization of clinical trials. The training will be useful for specialists of health care and preventive…

02 June – workshop “Life cycle of registration materials within the variation procedure, eCTD format”

23.04.2026 823

The focus is on practical issues of interaction with the Single Window and the Service Center, specifics of submitting registration dossier materials under the procedure for making…

(Enrollment closed). On 25 September 2026 we invite you to an online seminar on Good Clinical Practice (GCP): what ICH E6(R3) changes for clinical trials

On 31 July 2026, we invite you to the practical seminar “The Most Common Non-conformities Identified During Audits of Applicants’ Pharmacovigilance Systems. Development of a Corrective and Preventive Action Plan”

On 8 July 2026, we invite you to the online seminar “The Applicant’s Pharmacovigilance System. Current Requirements and Expected Changes”

19 June – certified online seminar “Good Clinical Practice (GCP). Regulatory framework for conducting clinical trials”

On June 10, 2026 we invite you to the workshop “Everything about generics and hybrids. What is similar and what is different. Requirements for demonstrating properties”. We look forward to your applications!

On 17 June 2026, we invite you to the seminar-training “HTA – a tool for assessing the value of medical technologies in terms of analysis of comparative clinical effectiveness and safety.” For the first time – in online and offline formats!

16 June 2026 – professional development seminar “The role of clinical trials in the development of medicinal products”, +3 points to the professional portfolio

23 June 2026 – workshop “Methodology for developing and implementing standards of medical and rehabilitation care”

09 June 2026 – CPD seminar “Organization of the trial site in a healthcare facility”, 3 points to the portfolio

02 June – workshop “Life cycle of registration materials within the variation procedure, eCTD format”

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