Training Services ANVISA RDC 16 Internal Auditor
ANVISA RDC 16/2013 internal auditor training from SGS – learn how to conduct medical device and product audits in compliance with Brazil’s new regulation.
The new National Health Surveillance Agency (ANVISA) RDC 16/2013 regulation outlines good manufacturing practices for medical devices and products used for in vitro diagnostics. It replaces regulations 686/1998, RDC 59/2000 and RDC 167/2004. As a result, you need to understand the principles of the new regulation and how it affects your organization. Our 16-hour course provides you with the knowledge you need to conduct audits to RDC 16/2013 requirements.
Why choose ANVISA RDC 16/2013 internal auditor training from SGS?
We can help you to:
- Learn about the ANVISA RDC 16/2013 regulation, including its approach, processes, terms and definitions, and history
- Understand and apply the detailed requirements of the regulation
- Develop your audit skills so you can plan, prepare, conduct, report and follow up consistent audits
Trusted ANVISA RDC 16/2013 training for internal auditors from Brazil’s leading course provider
As a world-leading training provider of ANVISA regulation training, we offer extensive expertise and experience in RDC 16/2013 requirements.
Our 16-hour course is conducted over two days and covers:
- Quality management systems
- Management responsibilities
- Resource management
- Realization of products and services
- System monitoring and improvement
This training is designed for anyone in charge of good manufacturing practice audits for manufacturers, importers and distributors of medical devices and products used for in vitro diagnostic use.
All participants must have previous knowledge of RDC 59/2000.
A certificate will be issued to participants who complete each module and achieve a score of at least 70% in the final exam.
To discuss how our ANVISA RDC16/2013 internal auditor training can benefit you and your organization, contact us today.