Understanding the complex global regulations in place for medical devices is a challenge if you are widening your market. Many different national regulations are in place, and focusing your business in different regions and countries needs careful planning to ensure that you meet the standards required.
Training on medical devices regulations is often needed to allow management to fully understand the business implications of a new market or regulation, to help customers and consultants write and amend quality documents, to assist in the compilation of technical files and as an introduction to new members of the quality or regulatory department.
SGS offers medical devices regulations training at auditor, quality professional, compliance engineer and general levels to help your organization widening your market.
Our specialists are located worldwide and we are the global benchmark for assurance, and leader of audit and certification services across a wide range of industries and sectors. Find out more.