Certifications

RDC 16:2013

RDC 16: 2013 – Technical Regulation on Good Manufacturing Practices (GMP – ANVISA), which establishes the requirements applicable to the manufacture of medical products and determines the methods and controls used in the design, purchasing, packaging, labeling, storage , distribution and post sales. Such technical requirements are intended to ensure that manufactured medical products are safe and effective in their application.

Certifications
Newsletter
Receive our alerts first hand!
Do you have any doubt?