SOPs & Templates

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Title Category Action
1 Call for Expression of Interest (EOI) for Regional Joint Medical Products Evaluation for Antimalaria Medicines Medical Products Dossier Evaluation and Registration Edit Details Delete
2 Regional Joint Assessment Procedure for Medicine Registration and Marketing Authorization of Medicinal Products Medical Products Dossier Evaluation and Registration Edit Details Delete
3 Sample Schedule for Allopathic Drugs for Registration and Re-Registration of Products Medical Products Dossier Evaluation and Registration Edit Details Delete
4 WAHO SOP on Change Control Quality Management Systems Edit Details Delete
5 WAHO SOP for backup and archiving Information Management Systems Edit Details Delete
6 WAHO SOP for Conducting Joint CAPA Verification Audit Good Manufacturing Practices and Inspections Edit Details Delete
7 WAHO SOP for conducting Joint GMP Inspection Good Manufacturing Practices and Inspections Edit Details Delete
8 WAHO SOP for Design Qualification Information Management Systems Edit Details Delete
9 WAHO SOP for Desk Review of inspection report Good Manufacturing Practices and Inspections Edit Details Delete
10 WAHO SOP for Disaster Recovery Plan Information Management Systems Edit Details Delete
11 WAHO SOP for Equipment Maintenance Quality Control Laboratories Edit Details Delete
12 WAHO SOP for Incident Reporting Information Management Systems Edit Details Delete
13 WAHO SOP for Installation Plan Information Management Systems Edit Details Delete
14 WAHO SOP for Installation Qualification Information Management Systems Edit Details Delete
15 WAHO SOP for IT Systems Implementation Life Cycle Information Management Systems Edit Details Delete
16 WAHO SOP for Laboratory Notebook Management Quality Control Laboratories Edit Details Delete
17 WAHO SOP for Product Qualification Information Management Systems Edit Details Delete
18 WAHO SOP for Proficiency Test & Inter-Laboratory Comparison Quality Control Laboratories Edit Details Delete
19 WAHO SOP for Risk Management Quality Control Laboratories Edit Details Delete
20 WAHO SOP for Test Plan Information Management Systems Edit Details Delete
21 WAHO SOP for Vaidation Plan Information Management Systems Edit Details Delete
22 WAHO SOP on Data Integrity Quality Control Laboratories Edit Details Delete
23 WAHO SOP on handling Out Of Specification (OOS) Test Results Quality Control Laboratories Edit Details Delete
24 WAHO SOP On Method Validation Quality Management Systems Edit Details Delete
25 WAHO SOP on Uncertainty of Measurement Quality Control Laboratories Edit Details Delete
26 WAHO Template Application form for Variation to a Registered Finished Medicinal Product Medical Products Dossier Evaluation and Registration Edit Details Delete
27 WAHO Template Assessment Report for Variation on Registered Finished Pharmaceutical Products (FPPS) Medical Products Dossier Evaluation and Registration Edit Details Delete
28 WAHO Template Audit Observation form Quality Management Systems Edit Details Delete
29 WAHO Template Change Control Evaluation form Quality Control Laboratories Edit Details Delete
30 WAHO Template Change Control form Quality Control Laboratories Edit Details Delete
31 WAHO Template Change Control Register Format Quality Control Laboratories Edit Details Delete
32 WAHO Template Client Complaint Form Quality Management Systems Edit Details Delete
33 WAHO Template Client Feedback form Quality Management Systems Edit Details Delete
34 WAHO Template Corrective Action Request Form Quality Management Systems Edit Details Delete
35 WAHO Template Document Change Note Quality Management Systems Edit Details Delete
36 WAHO Template Equipment History Card Quality Control Laboratories Edit Details Delete
37 WAHO template for communication with clients Medical Products Dossier Evaluation and Registration Edit Details Delete
38 WAHO Template Internal Audit Report form Quality Management Systems Edit Details Delete
39 WAHO Template Investigative Analysis Protocol Quality Control Laboratories Edit Details Delete
40 WAHO Template Non Conformance Report Quality Management Systems Edit Details Delete
41 WAHO Template Non Conformance Status Summary Quality Management Systems Edit Details Delete
42 WAHO Template OOS Investigation Checklist Quality Control Laboratories Edit Details Delete
43 WAHO Template OOS Investigation Report Form Quality Control Laboratories Edit Details Delete
44 WAHO Template OOS Notification Memo Quality Control Laboratories Edit Details Delete
45 WAHO Template OOS Pathway Quality Control Laboratories Edit Details Delete
46 WAHO Template OOS Result Register Quality Control Laboratories Edit Details Delete
47 WAHO Template OOS Trend Sheet Quality Control Laboratories Edit Details Delete
48 WAHO Template Screening Checklist – Generic Product Medical Products Dossier Evaluation and Registration Edit Details Delete
49 WAHO Template Screening Checklist – New Chemical Entity Medical Products Dossier Evaluation and Registration Edit Details Delete
50 WAHO Template Screening Checklist Application Submission Medical Products Dossier Evaluation and Registration Edit Details Delete
51 WAHO Template Screening Checklist for Module 1 Medical Products Dossier Evaluation and Registration Edit Details Delete