Directorate General of Drug Administration: (Allopathic Medicine)
Regulatory Affairs:
 Evaluation of the proposals of new projects of all systems of medicines from Directorate General of Drug Administration (DGDA).
 Issue and renewal of drug manufacturing licenses (Both Biological & Non-Biological) from Directorate General of Drug Administration (DGDA).
 Issue and renewal of retail and whole sale drug licenses from Directorate General of Drug Administration (DGDA).
 Registration and renewal of drug products from Directorate General of Drug Administration (DGDA).
 Submission & Approval of Product Price both IP & MRP Products from Directorate General of Drug Administration (DGDA)
 Inspection of Pharmaceutical establishments from Directorate General of Drug Administration (DGDA).
 Submission & Approval of Online Block list both online & software (Local & Export) for the import of raw- and packaging materials from Directorate General of Drug Administration (DGDA).
 Approval of indent for import of finished drugs from Directorate General of Drug Administration (DGDA).
 Submission, Surveillance and Pharmacovigillance activity from Directorate General of Drug Administration (DGDA).
 Submission & Approval of export licenses, FSC (Free Sales Certificate), GMP (Good Manufacturing Practices) Certificate & CPP (Certificate for Pharmaceutical Products.) from Directorate General of Drug Administration (DGDA).
 Submission & Approval of Marketing Authorization Certificate from Directorate General of Drug Administration (DGDA).
 Submission & Approval of Product Information Dossier (PID) according to WHO Guideline from Directorate General of Drug Administration (DGDA).
Purchase:
 To plan prepare and update suppliers or vendors list of Raw Material and other inventories required as per budget.
 To open L/Cs with bank & follow-up with suppliers for timely shipment of materials to run the production smoothly.
 To collect quotations at least three suppliers or vendors for purchase of Raw, Packaging & promotional and other materials and obtain management approval.
 To obtain prior clearance from Quality Assurance Department for all Factory inventories & Marketing Department for all promotional materials before issuing purchase order.
 To prepare & issue purchase order in ERP system both local and foreign with management approval.
 To identify & outsource all major suppliers of inventories required to run, the production at Factory with competitive prices both local and foreign.
 To maintain ideal ratio of inventor for major production and other levels of inventories based on budget & market demand.
 To arrange timely clearance of products from customs and communicate with C & F agents with Factory.

Trade Mark:
 Trade Mark & Registered Trademark approval from Department of Patents, Designs & Trademarks (DPDT)
Narcotics:
 Narcotics License & Drugs approval from Narcotics Department
Toll Manufacturing Work:
 All types of Toll Manufacturing activities
Bangladesh Energy Regulatory Commission (BERC)::
 Submission to the License waiver document from Factory engineering documents
Environment Department:
 NOC from Environment Department both online & off line.
Explosive Department:
 NOC from Explosive Department both online & off line.
 License from Explosive Department.

Brand: Area of Support