Kanchan Subhash Chandra Gond*

Graduate School of Pharmacy, Gujarat Technological University, Gandhinagar, Gujarat, India

*Corresponding Author: Kanchan Subhash Chandra Gond, Graduate School of Pharmacy, Gujarat Technological University, Gandhinagar, Gujarat, India.

Received: April 10, 2023; Published: May 15, 2023

Abstract

One of the key causes of the breast implant market is the rising prevalence of breast cancer around the world. Breast cancer has surpassed lung cancer as the most commonly diagnosed cancer worldwide, according to GLOBOCAN 2020. According to the World Health Organization, around 2.3 million women will be diagnosed with breast cancer in 2020, with 685,000 of them dying. In addition, over the last five years, over 7.8 million women have been diagnosed with breast cancer. Breast cancer was found to be so common in Asian women that it accounted for 22.9 percent of all cancer cases in women in 2020. The increased inclination and knowledge of women globally toward breast augmentation is another factor that is predicted to promote the market's growth.

 Keywords: Plastic Surgery; Breast Augmentation; Recombinant Surgery; Implants

References

1. Council EUR Lex.
2. French-Mowat Elaine and Joanne Burnett. “How are medical devices regulated in the European Union?” Journal of the Royal Society of Medicine1 (2012): S22-28.
3. Implants and Prosthetics.
4. Type of Breast implants American Society of Plastic Surgeons.
5. Implanted Medical Devices – A Huge Industry.
6. Saline, Silicone Gel, Alternative Breast Implant.
7. Saline Breast Implants: The Advanced Step-by-Step Guide.
8. Risks and Complication of Breast Implant.
9. Breast Implant Wikipedia.
10. Allergan Breast Implants.
11. European Union - OECD.
12. European Medicines Agency Wikipedia.
13. Mutual Recognition Agreements.
14. Europe Breast Implant Market.
15. Breast Implant Market.
16. Companies in the Global Breast Implants Market.
17. Medical Devices -EU Regulatory Framework.
18. Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices.
19. Directive 98/79/EC of the European Parliament.
20. CE Marking – European Commission.
21. CE Marking Wikipedia.
22. B Council Directive 93/42/EEC of 14 June (1993).
23. Coroneos Christopher J., et al. “Breast Implant Post approval Studies”. Annals of Surgery1 (2019): 3036.

Citation

Citation: Kanchan Subhash Chandra Gond. “A Study of Regulatory Requirement for Registration Process for Breast Implant Medical Devices as per European Medicinal Agency”.Acta Scientific Medical Sciences 7.6 (2023): 46-52.

Copyright

Copyright: © 2023 Kanchan Subhash Chandra Gond. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.