Developing Guidelines on Reporting Adverese Cosmetic Product Reaction for Notifier According to Cosmetics Act B.E.2558 (2015)

Main Article Content

Waelta Prapatsorn Prapatsorn

Abstract

According to Cosmetics Act B.E. 2558 (2015) the authority should set the Guidelines of Reporting on the Adverse Cosmetic Product Reaction for the notifer of cosmetics. This study aimed to conduct on the comparative study among the guidelines on reporting adverse cosmetic product reaction of the European Union (EU), ASEAN and Thailand. It was a document research and qualitative research.The ASEAN Guidelines and Forms on Reporting Adverse Cosmetic Product Reaction for the Industry was used to be the prototype for a  sub-group meeting among the staff of cosmetics Section and sub-committee meeting among  22 persons, consisting of the officials from the Food and Drug Administration, the representatives of the relevant government agencies, and private sectors. The draft of Guidelines and the Reporting Form were revised and asked the opinions the meeting of the manufacturers and importers of cosmetics. Then the comments from the meeting were used to improve the draft guidelines and reporting form for further benchmarking against the EU's,  ASEAN's  and Thailand‘s  reporting system.    The results showed that the guidelines for Thailand should include 6 sections which were Definitions, Types of Serious Adverse Cosmetic Reaction, Data collection in a Product Information File (PIF), Direction of reporting the Serious Adverse Cosmetic Reaction, Time to submit the report, and Penalty for violating the Guidelines. For the Form of collecting adverse cosmetics reaction. It was improved to be suitable for Thailand. After The guidelines issuance, the guidelines manual should be prepared for the notifiers to 1) recognize their duty, and responsibility for the Adverse Cosmetic Reaction 2) set up the surveillance program for managing the Adverse Cosmetic Reaction product sampling for analysis and data collection in a Product Information File (PIF) 3) The consumers to consult the medical professional for their Adverse Cosmetic Reaction.

Article Details

How to Cite
1.
Prapatsorn WP. Developing Guidelines on Reporting Adverese Cosmetic Product Reaction for Notifier According to Cosmetics Act B.E.2558 (2015). TFDJ [Internet]. 2018 Oct. 1 [cited 2024 Apr. 20];25(3):20-35. Available from: https://he01.tci-thaijo.org/index.php/fdajournal/article/view/148375
Section
รายงานการวิจัย

References

1. ASEAN Cosmetic Committee (ACC). (June 2005). A Guide Manual for the Industry : Adverse Event Reporting for Cosmetic Products.

2. Cosmetics Europe. (2016). Guidelines on the management of undesirable effects and reporting of serious undesirable effects in the European union.

3. สำนักงานคณะกรรมการอาหารและยา. ศูนย์เฝ้าระวังความปลอดภัยผลิตภัณฑ์สุขภาพ.แบบฟอร์มการรายงานอาการอันไม่พึงประสงค์ของผลิตภัณฑ์สุขภาพ.

4. พระราชบัญญัติเครื่องสำอาง พ.ศ. 2558, (2558, 8 กันยายน). ราชกิจจานุเบกษา. เล่ม 132 ตอนที่ 86ก, 5-25.

5. André, O. Barel., Marc, Paye., & Howard, I. Maibach. (2014). HANBOOK OF COSMETIC Science and Technology (4th ed ). Boca Raton, Flo: CRC press taylor & francis group.

6.THE EUROPEAN COMMISSION. (2017, February 10). Commission Regulation (EU) 2017/237 of 10 February 2017 amending Annex III to Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products. Official Journal of the European Union, p. L 36/12.

7. THE EUROPEAN COMMISSION. (2017, August 2). Commission Regulation (EU) 2017/1410 of 2 August 2017 amending Annexes II and III to Regulation (EU) No.1223/2009 of the European Parliament and of the Council on cosmetic product. Official Journal of the European Union, p. L 202/1-L202/3.

8. THE EUROPEAN COMMISSION. (2017, July6). Commission Regulation (EU) 2017/1224 of 6 July 2017 amending Annexes V to Regulation (EU) No.1223/2009 of the European Parliament and of the Council on cosmetic product. Official Journal of the European Union, p. L 174/16- L 174/18.

9. Harry, RG. (2000). Harry's Cosmeticology 8th Edition (2nd ed). Boston: Chemical Publishing Co. Inc.

10. European Commission. (2012). SUE REPORTING GUIDELINES.

11. European Commission. (2013). SUE FORM A: NOTIFICATION OF SUE BY RESPONSIBLE PERSON OR DISTRIBUTOR TO COMPETENT AUTHORITY.

12. Camp, RC. (1995). Business process benchmarking:finding and implementing best practices. Milwaukee, Wis: ASQC Quality Press.

13. โรแบร์, พอลล์ เจมส์. (2543). หลักการวิเคราะห์และเปรียบเทียบความสามารถอย่างเป็นระบบ.กรุงเทพฯ: มหาวิทยาลัยธุรกิจบัณฑิตย์.