1 | Cover letter to the Member Secretary |
2 | Application form for initial review |
3 | Proforma |
4 | Case report forms |
5 | Survey tools |
6 | Follow-up cards |
7 | Permission of using copyrighted proforma/ questionnaire |
8 | Complete protocol |
9 | CVs of all the investigators with relevant publications in the last five years |
10 | Informed consent document (ICD) in English as well as local language(s) (please refer to Annexure 3 of Tech4Health Foundation's SOP) |
11 | Case record form/questionnaire |
12 | In case of HIV testing/genetic screening, pre-test and post-test counselling forms |
13 | Recruitment procedures: advertisement, notices, if applicable |
14 | Patient instruction card, diary, etc., if applicable |
15 | Investigator’s brochure (as applicable for drug/biologicals/device trials) |
16 | Details of the funding agency or sponsor and allocation of funds, if applicable |
17 | A statement on CoI (Conflict of Interest), if there isn’t any conflict, it should state so in the CoI |
18 | GCP training certificate (preferably within the last five years) of investigators (in case of sponsored clinical trials) |
19 | Any other evidence relevant for research ethics, if applicable |
20 | List of all ongoing research studies under the PI supervision, if applicable |
21 | Undertaking with signatures of investigators |
22 | Regulatory permissions, as applicable |
23 | Relevant administrative approval(s) |
24 | MoU in cases of studies involving collaborations with other institutions, if applicable |
25 | Clinical trial agreement between the investigator and sponsors of the study, if applicable |
26 | Insurance policy, if applicable |