6-Hour Virtual Seminar on FDA Trends for Computer System Validation (CSV) Compliance and Enforcement
Product Id : 10039
Price Details
Upon completion of this session, attendees will have an understanding of
FDA compliance and enforcement as it relates to computer system
validation. They will understand how to develop the most robust
computer system validation compliance program, focusing on the critical
areas of interest to FDA. The attendees will have a good grasp of how
to identify potential weaknesses and findings, as well as how to make
recommendations for addressing and remediating them through risk
mitigation.
In particular, we will focus on best practices for
validating computer systems regulated by FDA and meeting compliance with
electronic records and electronic signatures (21 CFR Part 11). We will
also provide current FDA trends, including a focus on data integrity
issues in industry, which will be illustrated through industry examples.
The
webinar will cover what you need to do to prepare for an FDA audit, and
also the importance and steps required to be certain you have audited
all vendors of regulated systems appropriately.
Why you should attend
Effective and compliant computer system validation is critical to any
FDA-regulated organization. FDA has set forth very specific
requirements for meeting compliance, and a very prescriptive set of
enforcement actions to protect patient and/or consumer safety. This
course will enable you to best anticipate and prepare for FDA scrutiny,
understand your role during inspections and audits, and gain insight to
the level of enforcement associated with various findings, consent
decrees and warning letters. Examples from industry will be used as
case studies to illustrate these.
It is vital for regulated
companies to maintain a pulse on the regulatory environment in order to
fortify system validation efforts, as necessary, to meet FDA
expectations. It is the best practice to have a robust computer system
validation, continue executing against it consistently, and documenting
it thoroughly. By maintaining a strong and consistent computer system
validation program, companies can further build trust with FDA and the
consumers who rely on such oversight for protection.
Who Will Benefit
- Information Technology (IT) Analysts
- IT Developers
- IT Support Staff
- QC/QA Managers and Analysts
- Clinical Data Managers and Scientists
- Compliance Managers and Auditors
- Lab Managers and Analysts
- Computer System Validation Specialists
- GMP Training Specialists
- Business Stakeholders using Computer Systems regulated by FDA
- Regulatory Affairs Personnel
- Consultants in the Life Sciences and Tobacco Industries
- Interns working at the companies listed above
- College students attending schools and studying computer system validation, regulatory affairs/matters (related to FDA) or any other discipline that involves adherence to FDA regulatory requirements
- FDA Regulatory Oversight
- Computer System Validation (CSV)
- System Development Life Cycle (SDLC) Methodology
- Good “Variable” Practice (GxP) (Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Good Clinical Practice (GCP))
- GAMP 5 Software Categorization
- System Risk Assessment
- Requirements, Design, Testing
- Requirements Traceability Matrix (RTM)
- Validation Documentation
- 21 CFR Part 11 Compliance (Electronic Records/Signatures)
- Audit Preparation
- Most Common Problems with CSV
- Best Practices
During her career, Carolyn worked directly, or on a consulting basis, for many of the larger pharmaceutical companies in the US and Europe. She developed validation programs and strategies back in the mid-1980s, when the first FDA guidebook was published on the subject, and collaborated with FDA and other industry representatives on 21 CFR Part 11, the FDA’s electronic record/electronic signature regulation.