Courses

Analytical Method Validation

Stay Ahead of the Curve: Analytical Method Validation Under Good Laboratory Practices (GLPs)

Don’t Leave Accuracy to Chance: Master Analytical Method Validation in GLP!

John Fetzer

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

APR 22, 2025 (TUE)

MEDICAL DEVICE CYBERSECURITY FDA COMPLIANCE

Cybersecurity Compliance: Master the Latest FDA Guidelines for Medical Devices

Protect Patient Data and Ensure Compliance in a Rapidly Evolving Landscape!

John E Lincoln

1 Hr.| 10 AM PT - 11 AM PT | USD 229

APR 23, 2025 (WED)

MEDICAL DEVICE CYBERSECURITY FDA COMPLIANCE

6-Hour Virtual Bootcamp on Medical Device Cybersecurity: Shield Your Data, Ensure FDA Compliance, Lead with Confidence

Implement Advanced Risk Management, Develop A Robust SQA Plan, & Stay Ahead of Emerging Cybersecurity Threats!

Carolyn Troiano

6 Hrs.| 9 AM PT - 3 PM PT | USD

APR 23, 2025 (WED)

FDA 510 k Submission Process

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

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

APR 23, 2025 (WED)

Excel spreadsheet validation

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 Hrs.| 9 AM PT - 12 PM PT | USD 459

APR 23, 2025 (WED)

Data Integrity & Human Error

Data Integrity & Human Error: Ensuring Compliance and Accuracy in Life Sciences

Understand, Identify, and Eliminate Human Errors To Protect Data Integrity!

Ginette Collazo

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

APR 23, 2025 (WED)

Data Integrity and Privacy

Data Integrity & Privacy Compliance: Mastering 21 CFR Part 11, Annex 11, & GDPR

Ensure Regulatory Compliance and Secure Your Data in the Digital Era!

Carolyn Troiano

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

APR 23, 2025 (WED)

Quality Management 101

Quality Management 101: Optimizing Enterprise Maintenance with ISO Standards

Transform Maintenance With ISO 9001 Insights for Proactive, Quality-Driven Results!

John E Lincoln

1 Hr.| 10 AM PT - 11 AM PT | USD 229

APR 24, 2025 (THU)

Process Validation Essentials

2025 FDA & ISO Process Validation Mastery: Advanced Process Validation for Global Regulatory Alignment

Stay Ahead or Pay the Price – Learn Cutting-Edge Strategies to Prevent Costly Compliance Mistakes!

Jose Mora

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

APR 24, 2025 (THU)

What is Required for 21 CFR Part 11 Compliance?

Beyond Compliance: Perfecting 21 CFR Part 11 for FDA-Regulated Computer Systems

Future-Proof Your Compliance: Adapting to 21 CFR Part 11 in 2024!

Carolyn Troiano

90 Mins.| 10 AM PT - 11:30 AM PT | USD 229

APR 24, 2025 (THU)

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