Quality Forms
- Form-005 Non Component Run Sheet
- Form-010 Sample Request Form
- Form-015 Warehouse Information Form
- Form-020 Bin Sheet
- Form-025 Return to Bulk Store
- Form-030 Issue for Production
- Form-035 Example-Bulk Tablet Sampling Form
- Form-040 Physical Inventory Count Form
- Form-045 Warehouse Bin Sheet Reconciliation Form
- Form-050 Warehouse Periodic Inventory Count Sheet
- Form-055 Material Transfer Order Form
- Form-060 Material Transfer Order-Interim Production Form
- Form-065 Material Transfer Order-Reject Form
- Form-070 Material Transfer Order-Return form
- Form-075 Goods Receipt Slip
- Form-080 In-House Identification Label
- Form-085 Released Stickers
- Form-090 Sampled Stickers
- Form-095 Rejected Stickers
- Form-100 Sampled Partial Stickers
- Form-105 Sampling Label
- Form-110 Pallet Racking Damage Log form
- Form-115 Warehouse Racking Checklist
- Form-120 Printed Material Sample Sheet
- Form-125 Example-Batch Reconciliation Sheet for Tablet Packing
- Form-130 Validation Protocol Deviation Reporting Form
- Form-135 Pest Sightings Reports
- Form-140 Visitor Entry Into The Factory
- Form-145 Intermediate Bulk Container Cleaning Tag
- Form-150 Example-Logbook for Tablet Batch Documents
- Form-155 Checkweigher Weight Record
- Form-160 Example- Line Clearance, Opening and Cleaning form for Tablet Packing
- Form-165 Pallet ID Form
- Form-170 Shipper Label Format
- Form-175 Vacuum Leak Test – Hourly Form
- Form-180 Vacuum Leak Test – New Foil and PVC Roll Form
- Form-185 Balance Calibration Logbook
- Form-190 Dispensary Label Form
- Form-195 In Process Check – Shipper Form
- Form-200 In Process Check-Blister and Carton form
- Form-205 Employee Log Form
- Form-210 Goods Booking Slip
- Form-215 Partial Shipper Stickers
- Form-220 Material Purchasing Information Record
- Form-225 Purchase Order Form
- Form-235 Monthly Production Schedule Form
- Form-240 Finished Goods Batch With Impending Expiry
- Form-245 Laboratory Master File of Instruments
- Form-250 Finished Goods Register
- Form-255 Raw Material Register
- Form-260 Finished Goods Trend Card
- Form-265 Raw Material Trend Card
- Form-270 Laboratory and QA Document Log Sheet and Box Labels
- Form-275 Workbook Checklist
- Form-280 Reagent Storage Location Form
- Form-285 Prepared Reagent Label Form
- Form-290 Chemical Waste Disposal
- Form-295 Raw Material Retention Sample Register Log
- Form-300 Finished Goods Retention Sample Register Log
- Form-305 Laboratory Investigation and Report form
- Form-310 Raw Material Out of Specification Investigation form
- Form-315 Stability or Trial Card
- Form-320 Template of Certificate of Analysis
- Form-325 Secondary RM Reference Substance (SRMRS) Summery Sheet
- Form-330 Primary and Impurity Substance Summery Sheet
- Form-335 Expired Raw Material Form
- Form-340 Trial Checklist
- Form-345 Primary Reagent Ref. Substance (PRRS) Summery Sheet
- Form-350 SRMRS Label
- Form-355 In-Process SRMRS Label
- Form-360 PRRS Label
- Form-365 Master Document Change Control Form
- Form-370 Validation Discrepancy Form
- Form-375 Validation Project Log Form
- Form-380 Intermediate Bulk Container Identification Label
- Form-385 Vendor Audit Questionnaire
- Form-390 New Supplier Assessment Form
- Form-395 SOP Ready for Signing
- Form-400 Employee Signature Register
- Form-405 Complaint Investigation Report
- Form-410 Document Location in Satellite File
- Form-415 Library Log Form
- Form-420 Request for New Chemical Approval
- Form-425 Housekeeping Audit Checksheet for Laboratory
- Form-430 Housekeeping Audit Checksheet for Production Services
- Form-435 Housekeeping Audit Checksheet for Electrical & Mechanical Workshop
- Form-440 Housekeeping Audit Checksheet for Warehouse
- Form-445 EHS Workplace Instruction Checklist
- Form-450 Deviation Report Form
- Form-455 Incident or Investigation Report Form
- Form-460 Register of Contracts
- Form-465 Complaints Details Form
- Form-470 New Chemical Approval Certificate
- Form-475 Housekeeping Audit Checksheet for Dispensary
- Form-480 New Chemical Rejection Advice
- Form-485 Housekeeping Audit Checksheet for Tablet Production
- Form-490 Laboratory Testing Form For Customer Complaint Enquiry
- Form-495 Form Ready for Signing
- Form-500 Training Participant Log
- Form-505 Document Creation or Change Request
- Form-510 Product To Be Reworked
- Form-515 Goods Return for Rework Form
- Form-520 Material Transfer Order Form
- Form-525 Hazardous Chemical Assessment Checklist
- Form-530 Reading Compliance Form
- Form-535 GMP Agreement Log
- Form-540 Pallet Booking Information
- Form-545 Raw Material Sampling Log
- Form-550 Finished Goods Shipping Form
- Form-555 Example-Batch Documentation Checklist for Tablet Packing
- Form-560 Test and Retention Sample Log Book
- Form-565 QA Inspection Sheet
- Form-570 Process Data Collection Form
- Form-575 Incident Investigation Form
- Form-580 Incident Communication Form
- Form-585 Contents of First Aid Emergency Kits
- Form-590 verification of Assay Result Sheet
- Form-595 Bacterial Endotoxin Test Data
- Form-600 Maximum Valid Dilution and endotoxin Limit Calculations
- Form-605 BET Gel Clot Validation – Final inhibition and Enhancement Test
- Form-610 BET Gel Clot Validation – Preliminary inhibition and Enhancement test
- Form-615 TOC Analyser Calibration Worksheet
- Form-620 Validation For Bacterial Endotoxin Using Kinetic Chromogenic Analysis (KCA)
- Form-625 Sterile Area Sample Identification Checklist
- Form-630 Non Steaming Machine Record For Micro Lab
- Form-635 Daily Personnel Monitoring Logs for Sterile Areas
- Form-640 Sample Identification Checklist For Terminally Sterilised Products
- Form-645 Sterile Chart Log For Microbiology Laboratory
- Form-650 Checklist for Procedure for Entry into Sterile
- Form-655 Validation Record For Sterile Gowning Procedure
- Form-660 Daily Store Room Temperatures
- Form-665 Microbiological Integrity (Soup) Test
- Form-670 Aseptic Media Fill Information Sheet
- Form-675 Plant Water – Isolate Identification Record
- Form-680 Sterility Test Failure Investigation Form
- Form-685 Lal Gel-Clot Test Session Results
- Form-690 Microbiology Out of Specification (OOS) Investigation and Report Form
- Form-695 EHS Risk Profile
- Form-700 Labelling of Settle (Fallout) Plates
- Form-705 Impact Assessment Form Computerised System
- Form-710 Record Reliability Controls
- Form-715 Analytical Testing Report for Non Standard Testing QA Inspection Sheet
- Form-720 HPLC Records
- Form-725 Raw Material Evaluation Form
- Form-730 Sample Request Form for Stability Program
- Form-735 On-Going Stability Product Order Form
- Form-740 Monthly Check of Stability Samples Stored in Ovens
- Form-745 EHS Risk Profile
- Form-750 Conditional Release Form
- Form-755 Autoclave Wet Cycle Acceptance Review Criteria
- Form-760 Equipment Tag Out for Validation
- Form-765 Documentation Verification and Cycle review
- Form-770 Validation Cycle Review
- Form-775 Change control, deviation, preventative and corrective maintenance summary sheet
- Form-780 Autoclave Validation Protocol
- Form-785 Autoclave Validation Documents Checklist
- Form-790 Steam Penetration Air Removal (Bowie Dick) Test
- Form-795 Pressure Regulator Test for Autoclaves
- Form-800 Empty Chamber Test for Autoclaves
- Form-805 Vacuum Leak Test
- Form-810 Equipment Calibration Verification
- Form-815 Autoclave Cycle Parameters Recording Sheet Template – Dry Cycle
- Form-820 Autoclave Cycle Parameters Recording Sheet Template – Wet Cycle
- Form-825 Autoclave Calibration Verification Record
- Form-830 Biological Indicator Test Results Sheet
- Form-835 Autoclave Dry Cycle Acceptance Review Criteria
- Form-840 List of Permitted Personnel to Enter Filling Clean Rooms
- Form-845 Eye Test Record
- Form-850 Inspection of Goods on Delivery
- Form-855 OOS Verification for Raw Material ID Using NIR
- Form-860 Corrective and Preventive Action Form
- Form-865 Packaging Reconciliation form
- Form-870 Defective Product Inspection form
- Form-875 Sterilization In Place – Validation Protocol Plan Approval
- Form-880 Sterilization In Place –Vessel Execution Record
- Form-885 Sterilization In Place Validation – Vessel Diagram
- Form-890 Sterilization In Place Validation – Data Collection Table
- Form-895 Sterilization In Place Validation – Transfer Lines
- Form-900 Sterilization In Place Validation – Transfer Line Diagram
- Form-905 Sterilization In Place – Transfer Lines Execution
- Form-910 Critical Documentation Verification – Post Execution
- Form-915 Critical Documentation Verification – Pre Execution
- Form-920 Change Control Tracking Form
- Form-925 Change Review Form – Toll Customer
- Form-930 Risk Assessment Registry
- Form-935 Finished Product Audit Record – Blending, Tableting, Packaging and QC
- Form-940 Visual Inspection of Final Finished Product
- Form-945 QA Inspection and Disposition of Raw Materials Checklist
- Form-950 QA Inspection and Disposition of Incoming Goods Checklist
- Form-955 QA Inspection and Disposition of Raw Materials Pre-Purchase Samples Checklist
- Form-960 Quality Control Test Request and Results
- Form-965 Finished Product Retention Sample Record – Room Temperature
- Form-970 QA Antigen Retention Sample Record
- Form-975 Finished Product Retention Sample Log, 2 – 8°C
- Form-980 Raw Material Retention Sample Log
- Form-985 Component Retention Sample Log
- Form-990 Packaging Retention Sample Log
- Form-995 Retention Sample Location Log
- Form-1000 Antigen Production Sample Log