TANZANIA MEDICINES AND MEDICAL DEVICES AUTHORITY

ISO 9001: 2015 CERTIFIED

PUBLIC NOTICE

14^th January, 2021

INVITATION FOR COMMENTS ON A DRAFT OF THE TANZANIA MEDICINES AND MEDICAL DEVICES (GOOD STORAGE AND DISTRIBUTION PRACTICES) REGULATIONS, 2021

1. The Tanzania Medicines and Medical Devices Authority (TMDA) would like to inform our esteemed stakeholders and the general public that we have recently developed a draft of the Tanzania Medicines and Medical Devices (Good Storage and Distribution Practices) Regulations, 2021.
2. The Regulations lay down the requirements for the storage and distribution of medical products thoughtout the supply chain which aims in ensuring the quality and identity of medical products during all aspects of the distribution process which include, but are not limited to, procurement, purchasing, storage, distribution, transportation, repackaging, relabeling, documentation and record-keeping practices.
3. The purpose of this notice is to inform the public that TMDA is inviting comments on this draft document which will help to finalize it. Please compile your comments specifying the draft regulations you are commenting on as per an example given below.
   

   TEMPLATE FOR COMMENTS

   Title of the Document	The Tanzania Medicines and Medical Devices (Good Storage and Distribution Practices) Regulations, 2021
   Part	Page number, regulation no., sub-regulation no./line no.,	Comment and Rationale

   
   
   
4. The draft Regulations can be accessed by Click here