Duration: (4:23) ?Subscribe5835 2025-02-15T15:05:32+00:00
Biopractice FDAMD UDI Requirement
(4:23)
BioPractice FDA’s Premarket Requirements for Medical Devices
(5:18)
BioPractice FDA Medical Device Regulation An Intruduction
(5:13)
Biopractice FDA PMA Submissions – Contents, Process, Pitfalls
(4:8)
Biopractice New Concept for Risk Management
(5:)
Biopractice FDA Medical Device Regulation Design Control
Biopractice Webinar on Biosimilar Key Factors for Successful Uptake in The Market
(2:52)
Biopractice FDA Medical Device Regulations Labeling Requirements
(5:6)
Biopractice Best Practices for FDA Inspection
(6:56)
SYS-003 Management Review Procedure for ISO 13485:2016 updated for 2020
(56:30)
IQ OQ PQ | Process Validation | Equipment Validation | Equipment Qualification | Medical Devices
(10:16)
Medical Device Complaint Handling: MDR, Reports of Removals and Corrections
(1:35)
Complaint Handling in Compliance with FDA and ISO Regulations
(1:4:54)
FDA 101 for Medical Devices
(57:47)
Overview of the USA FDA Classification Process
(6:50)
Premarket Approval (PMA) Agreement with FDA for the Medical Device Companies
(46:45)
Week 9 : CONFOUNDING: INTRO
(10:36)
Complaint Handling in Compliance with FDA \u0026 ISO Regulation
(5:32)
Biopractice Good Distribution Practices
(4:59)
15417 FDAMD UDI Req chunk 1
(4:46)
BioPractice Recorded Webcast European approval of Biosimilar products wmv
(1:43)
Biopractice How to Write a Scientific Article
(4:42)
Biopractice Refresh Epidemeology
(4:57)
Biopractice How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare
(5:5)
Biopractice FDA Import Requirements
(4:34)
Biopractice Reconcile ICH GCP with Risk Based Monitoring
(5:38)
Biopractice Complaint Handling in Compliance with FDA \u0026 ISO Regulation
Biopractice Registries Latest FDA Trends
Biopractice Orphan Drugs Approve in EU \u0026 Int
BioPractice_FDA Medical Device Regulation - An Intruduction