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2024 г.
DRUG REGULATORY AFFAIRS - update | Training Course | 3 modules | 04.10.2024 – 06.12.2024 | Online event | In person Program Module 3
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Module 3 dated 6 of December, 2024
The event om 6th of December 2024 kicked off with an official welcome from Prof. Tatyana Benisheva and Prof. Dobriana Sidgimova. Prof. Benisheva emphasized the importance of the event as the final Module 3 for 2024, stressing the role of continuous learning and collaboration in the regulatory affairs sector and pointed out the upcoming event - 15 Anniversary of BADI - October 2025
Please read the summary of the presentations with the most important highlights of each of them. Nice reading here .......

Highlights of the presentations in English Language Module 3
Highlights of the presentations in Bulgarian Language Module 3
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Module 2 dated 22 of October, 2024 Program Module 2
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The event provided a platform for exchanging ideas and addressing the most pressing regulatory concerns, Artificial Intelligence (AI). 3 years is a transitional period for all devices Class II-IV and those with AI need to be recertified. Strategy in Drug Development was presented at FDA and EMA and the presentation is a good manual for those who would like to have a new start in the innovative industry. Pharmacovigilance is an important topic and the new changes from August 2024, Module XVI - Risk minimization measures (Rev.3) was a focus of the presentation. Safety of Biosimilars of 6 INN (Adalimumab, Bevacizumab, Trastuzumab, Rituximab, Infliximab, Etanercept) shows the insight of 6 INN of biosimilars to their reference produc. Regulatory frame on nonregistered products and Compassionate use in Bulgaria was another important topic. Read more
Highlights of the presentations in English Language Module 2
Highlights of the presentations in Bulgarian Language Module 2
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Program and CVs Module 1 04.10.2024 | Highlights before Module 1
Venue : Hotel Forum, Conference Hall Central 41 Tsar Boris III Blvd./ Sofia 1612, Bulgaria
On October 4th, BADI held Module 1 live with over 80 participants, including lecturers and moderators from the Bulgarian Drug Agency (BDA), the industry, and academia. The topics were dedicated to audits and inspections of pharmacovigilance (PV) and quality (QA) systems, signal management, reporting of adverse drug reactions by healthcare professionals, as well as the switch of medicines’ prescription status from OTC to prescription and vice versa, directly related to safety. Summaries of the presentations by the lecturers, along with their references, can be found in this document, which is prepared in English and in Bulgarian language (Highlights in Bulgarian and Highlights in English Language) please read below the links:
Highlights of the presentations in Bulgarian Language
Highlights of the presentations in English Language List of attendees
SESSIONS
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Teambuilding TIME
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19.06.2024 г.
On June 6, 2024 the Annual Congress of the Bulgarian Association for Drug Information (BADI) - Pharmaceutical Legislation was held in University Hospital "St. Ekaterina" | Aula "Prof. Dr. Alexander Chirkov". It is of great professional importance for BADI that this significant forum was attended by representatives of the pharmaceutical industry, academia, guests from the Ministry of Health and the Bulgarian Drug Agency, as well asspeakers - leading experts from Bulgaria and the EU. We are pleased to have the Minister of Health, Dr. Galya Kondeva, send a congratulatory address on the occasion of the Annual Congress of BADI, vice president of the BADI- Prof. Dobriana Sidjimova read to the wide audience. Photo Gallery
Program | CV Lecturers

06.06.2024 г.
On May 30 and 31, 2024 was held the limited two-day Тraining Course: FOUNDATION SKILLS IN DRUG MARKETING AUTHORIZATION PROCEDURES OF MEDICINAL PRODUCTS IN THE EU, WORKSHARING OF MPS, GMP, GDP, organized by Bulgarian Association for Drug Information (BADI), at University Hospital "Sveta Ekaterina", Hall 2. Speakers this year were established experts in the field of health care, who presented their presentations in a professional manner and shared their experience with the audience. Experts from Bulgarian Drug Agency (BDA) shared how the EMA Commissions work, as well as useful information for the authorization of medicinal products.
Program | CV Lecturers

30.04.2024 г.
On 24.04.2024, the exclusive training seminar was held on the topic: PRICING AND NEW MECHANISMS AFFECTING DRUG REIMBURSEMENT SYSTEMS IN THE EU, incl. in the R. BULGARIA, organized by the Bulgarian Association for Drug Information (BADI), with the joint participation of the National Council on Prices and Reimbursement of Medicinal Products (NCPRMP). The event discussed the Bulgarian and European legislation, regarding prices and reimbursement, and Regulation (EU) 2021/2282 on HTA and its implementation, as well as the National Health Insurance Fund policies. Lecturers in the training seminar were leading experts from the NCPRMP and the NHIF. Dr. Vladimir Afenliev - Director of the "Drug Policy" Directorate of the NHIF, presented the topic: "Updates in the treatment, reimbursement of medicines and possibilities of the Drug Policy of the National Health Insurance Fund", and representatives from the Council on Prices and Reimbursement of Medicinal Products, represented by the Chairman of the NCPRLP - Assoc. Silvia Terezova, Mag.- Pharm. Boryana Ivanova, Prof. Manoela Manova and Prof. Alexandra Savova presented the topics: "Pricing in the Republic of Bulgaria", "European legislation Regulation (EU) 2021/2282 on HTA" and " Implementation status Regulation (EU) 2021/2282 on HTA" . Special guests and participants of the event were representatives from the Ministry of Health, experts from the institutions, the Academy and the industry, who took an active part in the discussions, and the Vice Rector for Science and Accreditation at the Medical University - Sofia, sent a congratulatory address, which was read to the audience of the Forum from Deputy the Chairman of BADI - Prof. Dobriana Sidjimova.
Program | CV Lecturers

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