ComplianceOnline Webinar - Controlling Change to meet GMP Requirements
September 9, 2010(Ended)
Online Webinar
This change control webinar will discuss the change control activities and documentation required to meet GMP requirements.This webinar will provide valuable assistance to all regulated companies in evaluating their existing or anticipated change control activities and documentation requirements, especially in light of the changes in the FDA`s stance vis a vis industry compliance and past problems. It will help attendees understand and recognize the most common change control failings and their fixes, and assist in defining and recognizing changes.
Areas Covered in the Seminar:
- Defining a "change" and "change control".
- Tougher FDA Expectations / Requirements.
- Areas impacted.
- FDA "Hot Buttons".
- Design Control.
- Document Control; Archiving.
- Identifying "changes".
- Preventing negative changes and entropy.
- Maintain a ‘state of control’.
This information applies to personnel / companies in the Pharmaceutical, Medical Device, Diagnostic, Neutraceutical and Biologics fields. The employees who will benefit include:
- Senior management
- Regulatory affairs
- Quality Assurance / QAE
- Production
- Engineering, R&D, and software development and testing teams
Prices *
249 US Dollar
Exhibition
No exhibition
Organization
Categories
Concurrent events
- Verification of Pharmacopeia Methods - Webinar by GlobalCompliancePanel 2010
- Signal Detection and Data Mining - Webinar by GlobalCompliancePanel 2010
- Learning from Recent FDA Warning Letters Related to Computer Validation and Part 11 - Prepare Yourself for the upcoming FDA Part 11 Inspections - Webinar by GlobalCompliancePanel 2010
- Project Management Certification Study Group - Information Year 2010
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
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