Draft Guidelines and Application Form For Lot Release of Vaccines and/or Other Biological Products

The Food and Drugs Authority (FDA) wishes to inform its stakeholders and the general public that new Forms and Guidelines for Lot Release of Vaccines and/or Other Biological Products have been developed. 

As part of the stakeholder engagement process, the FDA invites comments and suggestions for improvement on the draft form and guidelines. Stakeholders are encouraged to submit their feedback from now until Wednesday, 12th March 2025, via email to fda@fda.gov.gh or info@fda.gov.gh.

Your input is valuable in shaping a regulatory framework that upholds consumer safety and industry best practices.