Quality Assurance and Laboratory Testing Divisionshall be responsible for enforcement of current Good Manufacturing Practices under the Act, and for testing or research of drugs and to perform other functions connected therewith. The Division will also perform the functions related to post marketing surveillance and shall be responsible for the evaluation, coordination and monitoring of safety, efficacy and quality of registered drugs and inactive materials including the clinical and toxicological study, drug recalls and with drawls, and to perform other functions connected therewith..
|Application Form||Statement of Quarterly Production||Quality Assurance||Download|
|Application Form||cGMP Performa (Schedule B-II)||Quality Assurance||Download|
|Notification||Import requirement for drugs for personal use of patient [under rule 13 of The Drugs (Import & Export) Rules, 1976, of Drug Act, 1976]||Quality Assurance||Download|
|Notification||Guidelines for authorized officers under special SROs for issuance of NOC or approval for import of drugs under the Drugs Act, 1976 and Rules framed thereunder||Quality Assurance||Download|
|Circular||Voluntary Recall Alert- Jumex (Selegling HCL) 5MG, Tablets, Batch No 7V001||Quality Assurance||Download|
|SROs||Provision For Import Of Anti-Cancer , Cardiac And Any Other Life Saving Drug (Unregistered) For Use In Hospitals And Institution||Quality Assurance||Download|
|SROs||SRO 577(I)/2016: Provision For Import Of Drugs As Donations By Any Agency In Pakistan||Quality Assurance||Download|