Policy & Advocacy.

Expert Review of Medicines and Medical Devices Regulation (MMDR)

AusBiotech has been closely involved in the Expert Review of Medicines and Medical Devices Regulation (MMDR), which seeks to streamline and enhance opportunities to improve regulation.

With the support of our AusMedtech committees and members, we have provided feedback to ensure that changes to the recommendations will carry benefits for companies working in the medicines and medical devices industry, reduce risk for patients and help build Australia’s global competitive advantage.

Read more about:

• Background and initial stages of the MMDR
• Therapeutic Good Administration (TGA)’s consultations and AusBiotech’s submissions