Visit the Membership page to understand the categories and benefits, then use this contact form or email us to begin the application process. The Board reviews all applications.
Can non-members attend GMDEF programmes?
Yes — most GMDEF webinars and events are open to the wider industry. Members receive priority access and discounted registration fees.
How do I submit a grievance or complaint?
GMDEF operates a formal grievance and complaint handling procedure (GMDEF-P1). Address grievances to the Secretariat marked for the Grievance & Complaint Handling Committee. All complaints are handled confidentially and within prescribed timelines.
How do I join a specific committee?
GMDEF members with relevant expertise can express interest in joining a committee. Contact the secretariat with your domain background and preferred committee. The Board appoints members based on expertise and capacity.
Can organisations sponsor GMDEF events?
Yes — GMDEF welcomes sponsorship and partnership enquiries from organisations aligned with the medical device sector. Contact us to discuss collaboration and visibility opportunities.
Does GMDEF provide consulting services?
GMDEF is a non-profit professional foundation and does not provide direct commercial consulting. However, our member network includes experienced consultants, auditors, and regulatory experts who can assist.
ISO 13485:2016 QMS Implementation for Medical Device Manufacturers
2025 — TBC
Faridabad / Online
SA comprehensive 2-day workshop on implementing and maintaining a QMS compliant with ISO 13485:2016, covering documentation, risk management, and audit preparation.
India Medical Device Regulatory Landscape 2025 — Annual Forum
2025 — TBC
New Delhi
GMDEF's flagship annual conference bringing together industry leaders, regulators, policymakers, and experts to review the medical device regulatory landscape and chart the path forward.
Cleaning Validation & Bioburden Testing for Medical Devices
Monthly Series
Online
A monthly webinar series covering AAMI TIR ST98, ISO 14644, residue testing, bioburden assay validation, and practical cleaning validation protocol writing.
