Gcp Finding

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At GCP Finding we pride ourselves at continuously learning and keeping up to date with the latest developments in clinical research and compliance issues that can potentially affect trial results or even patient safety. We have created 150 unique examples using live documents which cover various GCP aspects including: a) Informed Consent (39 Unique Findings) b) Investigational Product (05 Unique Findings) c) Source Documentation (27 Unique Findings) d) Case Report Form (28 Unique Findings) e) The Protocol Compliance (11 Unique Findings) f) Ethics Committee (09 Unique Findings) g) Study Logs and Forms (31 Unique Findings) Our GCP findings modules will help: Clinical Project Manager- Training team members on GCP findings and ensuring study is in compliant with GCP requirements Clinical Research Associate – Ensuring GCP findings are captured during site monitoring visit Clinical Trial Coordinator - To avoid GCP findings while completing study documents Clinical Investigator- Keeping investigative site compliant with GCP requirements FDA WARNING LETTERS: This module is crafted for those who are involved in conducting clinical trials, at sponsor or CRO or at the Investigator site. There are nearly 1300 pages which includes: a) Clinical Investigator/Sponsor Investigator – 220 FDA Warning Letters b) Institutional Review Board – 73 FDA Warning Letters c) Sponsor/Monitor/Contract Research Organization – 53 FDA Warning Letters For affiliation with our organisation write to info@gcpfinding.com
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