I will write validation master plan and sops for pharmaceuticals

Hello welcome to my Gig.

Your one-stop solution for cGMP-compliant pharmaceutical documents.

I will write a Validation Master Plan as per cGMP guidelines.

These include:

• Equipment Qualification.
• Method Validation.
• Process Validation.
• Cleaning Validation.
• Computer system validation
• Vendor Qualification.
• Water System Qualification.
• Periodic Review and Requalification
• Analyst Qualification

I will prepare all cGMP-compliant documents, protocols, and sops according to national and international guidelines.

• Equipment Qualification (IQ, OQ, PQ), (USP <1058>
• Calibration, and Maintenance
• Weighing of an analytical balance (USP <41>, USP<1251>)
• Preventive Maintenance
• Risk Assessment
• Change Control Management
• CAPA Management
• Handling of Out of Specification (OOS)
• Handling of Laboratory Incidents, Deviation management
• Glassware Cleaning Validation
• Access Management

I am ready to collaborate with you. Feel free to contact me before placing any orders or any doubts.

Thank you for considering my gig, and I look forward to working with you to enhance your business operations!

Have a good day.