- 1_Application Form For Initial Review [AF/03-008/01]
- 1.1_Protocol Summary Sheet Checklist of items [AF/04-008/01]
- 1.2_Application Form For Initial Review Of Case Study Case Series [AF/05-008/01]
- 2_Application Form For Re-submitted Protocol Review [AF/02-013/01]
- 3_Application Form For Continuing Review [AF/01-015/01]
- 4_Application Form For Protocol Amendment Review [AF/01-014/01]
- 5_Study Assessment and Report Form (Consolidated) [AF/01-012/01]
- 5.1_Study Assessment Form For Case Study and Case Series [AF/02-012/01]
- 5.2_Informed Consent Assessment Form (now consolidated into a single form# 5…… use form 5) [AF/03-012/01]
- 6_Assessment Report Form (now consolidated into a single form# 5…… use form 5) [AF/04-012/01]
- 7_Resubmitted Protocol Review Form [AF/01-013/01]
- 8_Format For Review Of Research Report [AF/02-015/01]
- 9_Final Report Review Letter Template1 [IRB/PN/yyyy/xxx]
- 10_Document Receipt Form [AF/02-008/01]
- 11_Contents Of Submitted Packages [AF/01-008/01]
- 12_Serious Adverse Event Report [AF/01-019/01]
- 13_Unexpected Adverse Event Summary Report [AF/02-019/01]
- 14_Safety Report Review Form [AF/03-019/01]
- 16_Deviation Non-Compliance Violation Record [AF/01-016/01]
- 17_Request For Revision Of an SOP [AF/05-001/01]
- 18_Study Termination Memorandum [AF/01-018/01]
- 19_Study Completion Report Form [F/01-016/01]
- 20_Document Request Form [AF/01-025/01]
- 21_Guide to Placebo Justification [ANNEX 11]