Services

MET Good's Consulting experts will work with your team to plan and develop your regulatory pre-market approval packages for the FDA's 510(k), IDE and PMA

MET Good Consulting offers a broad range of in-country experts to assist US Medical Device companies in planning, preparing, submitting and tracking regulatory approval packages throughout the Asia-Pacific region.

Need help designing and implementing your ISO 13485 compliant Quality System?  Our experts will work closely with your team to develop procedures that match your company culture.

Whether from a practice audit or from an FDA audit, our experts can help you to resolve your 483 non-conformaties.  For foreign medical device companies, we will serve as your FDA Agent and Official Correspondant.

MET Good Consulting offers a broad range of training classes and material tailored in content and complexity to address your company's needs.

Risk Management is basis medical device safety in regulatory processes around the world.  Our experts will train you, help develop your processes and assist in preparing your Risk Management report.