JD Supra

The QMSR Goes Live and FDA Implements a New Medical Device Inspection Technique

On February 2, 2026, the U.S. Food and Drug Administration’s long-awaited harmonization of the medical device good manufacturing practice ...
Mena FN

Documentationconsultancy.com has Re-launch ISO 13485 Documentation kit

(MENAFN- Online PR Media) Free Demo of this readymade ISO 13485 document package guides buyers to understand the actual requirements and templates covers in the most demanding documents. Online PR ...
Business Wire

Research and Markets: ISO 13485-2003 Quality and Procedure Manual For Medical Devices

DUBLIN--(BUSINESS WIRE)--Dublin - Research and Markets (http://www.researchandmarkets.com/research/cgb5zw/iso_134852003_qua) has announced the addition of the "ISO ...
Mena FN

Punyam Academy Has Launched An ISO 13485 Lead Implementer Training E-Learning Course

(MENAFN- ForPressRelease) Punyam Academy, a reputable name in the industry as well as a leading name in E-learning training and a certification provider for ISO standards and other types of management ...
MD&M East

Benefits of ISO 13485 Certification for Medical Device Manufacturing

The medical device sector must meet stringent regulatory requirements plus convince potential customers that they make reliable, safe products. Having a strong commitment to quality can help customers ...