Online conference “Technical Regulation on cosmetic products: How to adapt to the new requirements and rules for manufacturers, importers and distributors”

Details:

• 
  Date: September 12, 2024
• 
  Time: from 10:00 to 14:00 Kyiv time
• 
  Event adress: Online
• 
  Language of the event: Ukrainian
• 
  Speakers:

  • Moderator, Yevheniia Lukianchuk, Head of the Weekly Pharmacy Weekly
  • Moderator, Pavlo Kharchyk, President of the AMOMD Association
  • Moderator, Daria Bondarenko, Executive Director of the AMOMD Association
  • Tatiana Ivanova, Audit Product Manager, Proxima Research International
  • Maksym Bagrieiev, Managing Partner of Cratia
  • Oksana Oliynychuk, Head of FMCG Department at Cratia
  • Tetiana Remzhyna, Head of Department of the accredited certification body “UNI-CERT”
  • Tetiana Pazerska, Lead Specialist of the Department for Medical Devices, Cosmetics and Registration of Medicines and Disinfectants of the Pharmaceutical Department of the Ministry of Health of Ukraine
  • Volodymyr Chekalin, Head of the Department of State Supervision of Medical Devices Circulation of the State Service of Ukraine on Medicines and Drugs Control
• 
  Cost:

  • Early bird price - UAH 5,900.00 including VAT - is valid until 05.09.24 inclusive. From 06.09.24 - 9 900,00 UAH including VAT

In the event:

1. Introductory speech
2. Relevance of the event, reasons and consequences of legislative changes
3. Overview of the cosmetics market in Ukraine: key trends and prospects
4. Transition period: how to import and put into circulation cosmetic products by 03.08.2026
5. Labeling and necessary documents for the transition period
6. Prerequisites and consequences of the adoption of the regulation, how the Ukrainian market will change
7. Legislative acts applicable together with the Technical Regulation
8. Actions to be taken under the Technical Regulation
9. How to distinguish between a cosmetic product, a medicinal product and a medical device
10. Requirements for the composition of a cosmetic product
11. Who is the Responsible Person, what are their duties and responsibilities
12. Labeling - how the packaging of cosmetic products will change
13. New documentation: file with information and report on the safety of the cosmetic product
14. Requirements of other technical regulations
15. Notification on the cosmetic portal of the Ministry of Health
16. Post-marketing
17. Scope of GMP or DSTU EN ISO 22716:2015
18. Sections of the good manufacturing practice standard
19. Sequence of development and implementation of good manufacturing practice
20. Requirements for documentation
21. Requirements for audits
22. GMP compliance is the responsibility of the responsible person
23. Dialogue with the regulator: discussion of open issues
24. Technical regulation and notification of cosmetic products
25. State supervision over the circulation of cosmetic products
26. General discussion and answers to questions from the audience
27. Summarizing the results

SIGN UP