We understand industry’s need of multiple documents and guidelines. We have created this page exclusively for our users, so that they can get all the relevant important information at one place.
- Indian Ayush GCP Guidelines
- E6(R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1), Guidance for Industry
- Guidance for Industry: Electronic Source Data in Clinical Investigations
- Use of Electronic Informed Consent (Q&A)
- CFR FDA 314
- CFR FDA 312
- CFR FDA 56
- CFR FDA 50
- CFR FDA 11
- Schedule Y
- E6 GCP Guidelines
- E9 GCP Guidelines
- ICMR Guidelines
- Indian GCP Guidelines
- CDSCO Guidance for Industry
- CT Inspection Guidelines (DCGI)