regulatory affairs
Hello! Good day friends,
It’s me Saif ULLAH Khan here, I’m associated with healthcare industry since 1992. If you are looking for quality professional work in my field at reasonable cost, I’ll do it for you
Planning a New Pharmaceutical Manufacturing unit
- Land selection Pharmaceutical Manufacturing unit according to DRAP requirements.
- Site approval
- Layout development & approval
- DML inspection after erection of building
- Manufacturing machinery procurement and installation
- QC Lab equipment requirement & installations
- ERP Software to control/monitor inventories/production& Sales etc.
Holding DML
1) New Registration of Human use product
- New molecule/dosage form
- Me Too Product (A composition already registered in Pakistan)
2) New Registration of Veterinary use products
- New molecule/dosage form
- Me Too Product (A composition already registered in Pakistan)
3) Renewal of DML
4) Change in QCM
5) Change in Production in charge
Have DSL & intended to market imported products
1) New Registration of Human use product
- New molecule/dosage form
- Me Too Product (A composition already registered in Pakistan)
2) New Registration of Veterinary use products
- New molecule/dosage form
- Me Too Product (A composition already registered in Pakistan)
Already have registered product and are active in market
- Renewal of registration
- Correction in formulation/composition
- Price hardship case
- Additional Pack size