• 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-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 InProcess Check – Shipper Form
• Form-200 InProcess 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 Validation Protocol Deviation Reporting Form
• 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