Duration: (4:37) ?Subscribe5835 2025-02-21T10:22:15+00:00
Biopractice FDA PMA Submissions – Contents, Process, Pitfalls
(4:8)
BioPractice FDA Medical Device Regulation An Intruduction
(5:13)
Biopractice FDA Import Requirements
(4:34)
BioPractice FDA’s Premarket Requirements for Medical Devices
(5:18)
Biopractice FDA Medical Device Regulation Design Control
Biopractice Best Practices for FDA Inspection
(6:56)
Biopractice Best Practices for FDA's Investigating Deviations
(6:32)
Biopractice Understanding the Mindset of an FDA Employee
(3:42)
Biopractice Webinar on Best Practices for FDA's Investigating Deviations
CAPA | Corrective Action Preventive Action | non conformance - corrective and preventive action
(10:1econd)
FDA Inspection Do and Don't List
(23:50)
How Biomarkers Can Improve the Drug Development Process
(5:47)
Best Practices for Investigating Quality Deviations
(26:54)
How to Prepare a Medical Device 510k Submission for FDA | Rob Packard | Joe Hage
(1:34:30)
How to Prepare for Your Next FDA Inspection
(59:31)
Biopractice FDA Medical Device Regulations Labeling Requirements
(5:6)
Biopractice Registries Latest FDA Trends
BioPractice : FDA’s Premarket Requirements for Medical Devices
Biopractice Complaint Handling in Compliance with FDA \u0026 ISO Regulation
Biopractice How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare
(5:5)
Biopractice FDA Purple Book Classification
(4:37)
Biopractice Webinar : Complaint Handling in Compliance with FDA \u0026 ISO Regulation
Biopractice FDAMD UDI Requirement
(4:23)
15312_Registries_Latest FDA Trends
(5:24)
1542_Understanding the Mindset of an FDA Employee
(3:55)
How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare