Documentation in pharmaceutical project takes a lot of time, effort and manpower. Months are spent on document creation and review, even then the documents are not completed.Our ready to use documents save time as well as manpower. It helps to start the production within time. It is beneficial for your company because in the business Time is Money.
Pharmaceutical Documents
SIte Master File - SMF
Validation Protocol Templates
Quality Assurance: Standard Operating Procedures
| SKU ID | Document Title | Format | Price (₹) | Buy |
|---|---|---|---|---|
| QA-SOP-1 | SOP of SOP (SOP on SOP) in Pharmaceuticals | MS-Word | ₹/ | Add to cart |
| QA-SOP-2 | Preparation of Site Master File, Manuals and Master Plans | MS-Word | ₹/ | Add to cart |
| QA-SOP-3 | Standard Operating Procedure on Validation and Qualification Procedure for Facility, Utility, Equipment and Process | MS-Word | ₹/ | Add to cart |
| QA-SOP-5 | Preparation of BMR and BPR | MS-Word | ₹/ | Add to cart |
| QA-SOP-6 | Quality Management Review | MS-Word | ₹/ | Add to cart |
| QA-SOP-7 | Standard Procedure for Line Clearance in Pharmaceutical | MS-Word | ₹/ | Add to cart |
| QA-SOP-8 | Preparation, Approval and Revision of Master Formula Record | MS-Word | ₹/ | Add to cart |
| QA-SOP-9 | Status Labeling | MS-Word | ₹/ | Add to cart |
| QA-SOP-10 | Movement of Batch Documents | MS-Word | ₹/ | Add to cart |