Courses
Mastering Medical Device Quality Bootcamp: Integrating and Excelling with 21CFR 820 & ISO 13485 in 2024
Empowering Excellence in Quality Compliance: Your Gateway to 2024’s Medical Device Standards!
Charles H. Paul
Cut Through the Complexity: Simplify 21 CFR Part 11 Compliance for Seamless Computer System Validation
Learn from the Experts: Master 21 CFR Part 11 Compliance and Actionable Strategies in 3 Hours!
Carolyn Troiano
Cybersecurity Compliance: Master the Latest FDA Guidelines for Medical Devices
Protect Patient Data and Ensure Compliance in a Rapidly Evolving Landscape!
John E Lincoln
Navigating FDA 510(k) Submissions: How to Sidestep Common Mistakes and Ensure Approval
Learn From the Pros to Get it Right the First Time and Get Your Product to Market Faster!
Charles H. Paul
How to Stop Spreadsheet Nightmares: Master Risk-Based Validation of Spreadsheet Applications
Elevate Your Expertise: Streamline Validation, Secure Data, and Excel in Compliance!
Carolyn Troiano
3-Day Virtual Boot Camp on Mastering Computer System Validation (CSV) – Your Path to CSV Mastery!
Overwhelmed by Latest CSV Demands? How About a 3-Day Roadmap to Clarity?
Carolyn Troiano
Fast-Track FDA Approvals: Mastering NDAs, INDs, and Drug Manufacturing Standards
Are FDA Approval Complexities and Multi-State IND Compliance Challenges Creating Critical Bottlenecks in Your Pipeline?
John E Lincoln
CAPA Under the FDA Lens: Why Do CAPA Systems Fail, and How Can You Ensure Yours Doesn’t?
Learn from Real CAPA Failures and Master CAPA Best Practices to Satisfy FDA Expectations!
Charles H. Paul
Data Integrity & FDA Governance: Modern Strategies for Regulated Computer Systems
Empower Your Compliance: Proactive Strategies for System Integrity & Compliance!
Carolyn Troiano
Quality Management 101: Optimizing Enterprise Maintenance with ISO Standards
Transform Maintenance With ISO 9001 Insights for Proactive, Quality-Driven Results!
