Medical device regulatory requirements training from SGS – helps your personnel understand medical device regulatory requirements, including Medical Device Directive 2007/42/EC, Japan's Pharmaceutical Affairs Law (JPAL), and the Canadian Medical Devices Conformity Assessment System (CMDCAS).
Whether you are a manufacturer or provider of medical products, devices, components and services, you need to meet a range of complex regulatory requirements, such as JPAL, CMDCAS and Directive 2007/42/EC. So how can you bring new and improved products to the market quickly, while meeting the highest quality standards and all relevant global regulations?
Why choose medical device regulatory requirements training from SGS?
Our one-day course can help you:
- Provide your personnel with an understanding of medical device regulatory requirements
- Understand Directive 2007/47/EC, JPAL and CMDCAS requirements
The trusted medical device regulatory requirements course from Singapore’s leading training provider
As a leading provider of medical device regulatory requirements courses in Singapore, we offer you unrivaled expertise and experience in helping personnel to understand Directive 2007/47/EC, JPAL and CMDCAS requirements.
Contact us today to learn more about our medical device regulatory requirements training.