Modules | CRAMbridge

An Interactive Guide to Good Documentation Practice
Personnel Qualification and Training in GxP Environments
Compliance Monitoring Procedures for Good Laboratory Practice : OECD 2
Conduct of Laboratory Inspections and Study Audit : OECD 3
Compliance of Laboratory Suppliers with GLP Principles : OECD 5
Application of the GLP Principles to Field Studies : OECD 6
Application of the GLP Principles to Short Term Studies : OECD 7
Role and Responsibilities of the Study Director in GLP Studies : OECD 8
Preparation of GLP Inspection Reports : OECD 9
The Role and Responsibility of the Sponsor in GLP Studies: OECD 11
Requesting & Carrying Out Inspections /Study Audits in Another Country : OECD 12
Application of the Principles of GLP to in vitro Studies : OECD 14
Guidance on the GLP Requirements for Peer Review of Histopathology : OECD 16
Application of GLP Principles to Computerised Systems : OECD 17
Relationship between the OECD Principles of GLP and ISO/IEC 17025 : OECD 18
Management, Characterisation and Use of Test Items: OECD 19
Guidance for Review of the GLP Status of Non-Clinical Safety Studies : OECD 20
Possible Influence of Sponsors on Conclusions of GLP Studies : OECD 21
GLP Data Integrity : OECD 22
Quality Assurance and GLP : OECD 23
Quality Improvement Tools and GLP : OECD 24
Efficacy Guideline for Good Clinical Practice ICH E6(R2)
New Drugs and Clinical Trial Rules, 2019 (CDSCO)
Clinical Data Safety Management