Regulations

Keeping your staff and wider organization up to date with the ever changing legislation, regulations and standards that apply to your products is a challenge. Understanding existing requirements is vital, knowing about upcoming changes and anticipating new requirements could make the difference between success and failure.

SGS has an in-depth knowledge of regulatory issues at both an international and local level. We are dedicated to giving you access to that knowledge and the experience we have of applying it in organizations across the globe. In addition, with an international network of training personnel we are your ideal partner to keep your staff up to date with regulatory compliance updates.

Our experienced teams can audit your manufacturing compliance with a number of regulations specifically for medical devices, including the 93/42/EEC Medical Devices Directive and the 98/79/EC In Vitro Diagnostic Medical Device Directive. Our certifications ensure that your products are safe and can be released into the market, supported with all necessary technical documentation.

The right medical certification at the right time is the key to winning new contracts, launching new products and entering new markets. Partnering with SGS gives you access to our global network of auditors and regulatory compliance experts. Call us now to discover more.