Software Verification and Validation Planning and Implementation 2012
March 6, 2012(Ended)
Online Webinar
Software Verification and Validation Planning and Implementation is a webinar that covers topics such as:
- Tougher FDA Expectations / Requirements
- Recent industry failures
- An FDA "Model"
- Roles of Verification and Validation
- A Brief Overview of 21 CFR Part 11
- A Typical Software V&V Protocol / Test Report
- Expected Regulatory Deliverables
- Legacy, Hybrid, New and ER / ES Systems
- Complementary Guidelines, e.g., GAMP
Software Verification and Validation Planning and Implementation brings together attendees fromPharmaceutical, Medical Device, Diagnostic, Neutraceutical and Biologics fields including Regulatory affairs, Senior management, Production / QAE, Quality Assurance, Engineering, R&D, and software development and testing teams.
Prices *
299 US Dollar
Exhibition
No exhibition
Organization
Categories
Concurrent events
- When FMLA ends and ADA begins. The FMLA/ADA Crossover: Coordination, Management, and Compliance Strategies 2012
- Audit/Inspection Preparedness for Clinical Research/Site Coordinators 2012
- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada 2012
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
Articles/News/Press releases
