We at Jansal provide assistance to our clients to prepare the documentation required for equipment requalification in Pharmaceutical and food Industry. We ensure that your plant meets your business objectives while being fully compliant with the latest Good Manufacturing Practice regulations and standards.
Documentation preparation for:
- Qualification Protocols Writing and Execution
- Installation, Operational and Performance Qualification for Manufacture, processing related to various equipment and utility equipment
- Validation Master Plan
- Commissioning Plan
- Witnessing of Supplier Testing Activities (FAT/SAT support)
- Inventory of Process Equipment and Utilities
- User Requirement Specifications
- Clean Room Qualification
- Temperature Mapping Services
