Investigational product accountability log

Investigational product accountability log NCR working edition 1.0 | Qualified review pending PURPOSE Reconcile product receipt, dispensing, returns and disposition. BEFORE USE Confirm applicability, responsible authors/reviewers and controlling study/authority requirements. Replace bracketed fields and remove completion instructions only after review. This working document is not an approved clinical or regulatory submission. DOCUMENT CONTROL Study: [protocol identifier] Site or organisation: [name] Version / effective date: [complete after approval] Prepared by / reviewed by: [appointed people] The remaining pages contain the working fields and completion guidance.