On March 27, 2025, the FDA, through the Center for Device Regulation, Radiation Health, and Research (CDRRHR), will hold a Virtual Public Consultation to present the proposed Administrative Order (AO) titled “Guidelines for Good Storage and Distribution Practices for Medical Devices.”
The consultation will be conducted via Microsoft Teams and will be open to representatives from the medical device industry. A total of 75 slots are available, with a limit of one representative per company.
Key Details:
- Receiving Authority: FDA-CDRRHR
- Submission Process: Stakeholders may submit comments, suggestions, or clarifications to the FDA-CDRRHR before the finalisation of the AO.
- Attendance: One representative per company, limited to 75 slots.
Implications for Stakeholders:
There are no immediate impacts on stakeholders. However, participating in the consultation and providing feedback may influence the final version of the guidelines.
For more information, refer to the official notice: https://tinyurl.com/4kshut34.
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