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2019 - FDA Compliance and Clinical Trial Computer System Validation
Date2019-02-27
Deadline2019-02-27
VenuePalo Alto, USA - United States 
KeywordsFDA compliance training; Gcp training; gxp compliance; System Development Life Cycle
Topics/Call fo Papers
FDA GxPs
Computer System Validation (CSV) Methodology
System Development Life Cycle (SDLC) Framework
Risk Management
GAMP 5
Compliance Strategy
Cost vs. Compliance
Industry Best Practices
Policies and Procedures
Training
Leveraging Vendors
Computer System Validation (CSV) Methodology
System Development Life Cycle (SDLC) Framework
Risk Management
GAMP 5
Compliance Strategy
Cost vs. Compliance
Industry Best Practices
Policies and Procedures
Training
Leveraging Vendors
Other CFPs
- Establishing a Medical Device Security Program
- Project Management for Computer Systems Validation
- How To Establish an Effective Chief Compliance Officer's (CCO) or Chief Risk Officer's (CRO) Function - Organization and Responsibilities
- BioSciences 2019 Conference Invitation
- ISSRD - International Conference on Recent Developments in Social Science and Business Management (ICRDSSBM)
Last modified: 2019-01-25 02:58:36