Complying with Computer and Software Validation Requirements
Training Overview
Improve Your Ability to:
- Validate computer and software systems and save money by discovering defects prior to production
- Determine what needs to be validated and how much validation is enough to ensure regulatory requirements are met
- Address FDA expectations for legacy systems and off-the-shelf software and avoid costly regulatory consequences
- Re-format database and ensure data is compatible with a new environment
- Create and execute a master validation plan to define the performance requirements of your system
- Generate and maintain adequate IQ/OQ/PQ documentation
- Audit software vendors effectively and efficiently to avoid integrating deficiencies of outside work
- Implement proven solutions for issues such as data integrity and security, document traceability and change control and create an easily navigated system
- Anticipate FDA field investigators' hot button issues and avoid regulatory enforcement actions
PTi international is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmaceutical education. Participants will receive a maximum of 14 hours (1.4 CEUs) of continuing education credit for full participation in the two-day training. ACPE # 326-000-06-023-L04, Initial release: 07/2006.
Booking Options
This course is available exclusively as an onsite training solution. To discuss a solution that fits your organization's needs, objectives, schedule and budget, contact a PTi Client Solutions Manager at 800-303-8194 or OnSiteSolutions@pti-international.com.