Medical Devices
How to Investigate Environmental Monitoring Excursions
Gerry O'Dell
Price:Medical Devices
BREXIT ? What's Changing for Life Science Product License Holders/M...
Robert J. Russell
Price:Medical Devices
Best Practices for FDA and Iso 13485 Corrective Actions
Carolyn Troiano
Price:Pharmaceutical
Regulatory Inspections - How to prepare for a visit from an FDA Aud...
Denise Wrestler
Price:Medical Devices
US FDA Medical Device QSR, 21 CFR 820 and Quality Management System
John E. Lincoln
Price:Pharmaceutical
Learning from Recent FDA Warning Letters Related to Part 11 and Com...
Dr. Ludwig Huber
Price:Medical Devices
Demonstrated Techniques to a Successful 510k Submission
Mercedes Massana
Price:Medical Devices
Management Responsibilities for QSR Initiative
Dan O'Leary
Price:Pharmaceutical
5-hr Virtual Seminar: Qualification and Control of Suppliers and Co...
Howard Cooper
Price:Medical Devices
How to Make Sure Your Foreign Vendors are FDA Compliant and Stay th...
Joy L. McElroy
Price:Medical Devices
Understanding the Brazilian Regulatory Environment for Medical Devices
Claudia De Lucca Mano
Price:Medical Devices
Cybersecurity Exploitation Recovery for Medical Device Software
Casper Uldriks
Price:Pharmaceutical
4 Hrs Virtual Seminar: Latin America Regulatory Compliance Requirem...
Robert J. Russell
Price:Medical Devices
Internal GMP Audit Program - Execution and Communication
Ronald Torlini
Price:Medical Devices