KYA 1348 - Principles and guidelines for good practice in the distribution of medical devices in accordance with the requirements of DY8d/G.P. Oik/1348
What is EIA 1348?
Ministerial Decision 1348 sets out the mandatory requirements to be met by companies active in the marketing and distribution of medical devices.
Compliance according to KYA 1348 is mandatory and the documentation of compliance is done by issuing a relevant certificate by a notified, for medical devices, Certification Body.
Benefits – Advantages of the EIA 1348
- A business that proceeds to comply with EIA 1348 will reap multiple benefits, including:
- Compliance with legislative requirements.
- Reputation and prestige for the company.
- Safe Products
- Improved service/product quality.
Why choose us?
- Expertise and Experience:Many years of experience in the development and implementation of quality management systems.
- Customized solutions: Customized solutions that meet the needs of your business.
- Support and Guidance: Ongoing support from initial assessment to final implementation and beyond.
