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 | ₹30 | Buy Now |
| QA-SOP-2 | Preparation of Site Master File, Manuals and Master Plans | MS-Word | ₹30 | Buy Now |
| QA-SOP-3 | Standard Operating Procedure on Validation and Qualification Procedure for Facility, Utility, Equipment and Process | MS-Word | ₹30 | Buy Now |
| QA-SOP-4 | CONDUCTING OF STABILITY STUDY | MS-Word | ₹40 | Buy Now |
| QA-SOP-5 | Preparation of BMR and BPR | MS-Word | ₹/ | Buy Now |
| QA-SOP-6 | Quality Management Review | MS-Word | ₹/ | Buy Now |
| QA-SOP-7 | Standard Procedure for Line Clearance in Pharmaceutical | MS-Word | ₹/ | Buy Now |
| QA-SOP-8 | Preparation, Approval and Revision of Master Formula Record | MS-Word | ₹/ | Buy Now |
| QA-SOP-9 | Status Labeling | MS-Word | ₹/ | Buy Now |
| QA-SOP-10 | Movement of Batch Documents | MS-Word | ₹/ | Buy Now |