-: Greetings from Parsan Engineers & Consultants :-
Parsan has recently started taking up the task of auditing new and existing facilities to ensure that their construction as well as operations follow cGMP standards followed by national and global regulatory bodies. Some manufacturing facilities to prepare all GMP documents and our personnel have participated in the GMP pharma project audit of the company. Auditing involves verification of documents and facilties to make sure that they conform to current regulatory norms.
What We Offer of audit includes:
- Manufacturing Sites
- Warehouse Capacities
- Technological Capacities
- Review Previous Health Authority Inspections
- Inspection of QC facilities and capabilities
- Others, such as effluent treatment systems, etc.