GlobalCompliance Panel
7.9K subscribers
1:10
Professional Courses | List of Training Courses - Seminars
GlobalCompliance Panel
1.6K views • 7 years ago
0:12
successfully completed seminar on "The New Clinical Trials Regulation 2017"
GlobalCompliance Panel
197 views • 7 years ago
0:39
How to build a complete Safety, Health & Environment Management System 2017
GlobalCompliance Panel
468 views • 7 years ago
0:35
successfully completed seminar on Statistics for the Non-Statistician
GlobalCompliance Panel
321 views • 7 years ago
1:29:36
Understanding Attribute Acceptance Sampling including Z1 4 and c=0 Plans
GlobalCompliance Panel
11K views • 7 years ago
1:19:59
Requirements Contents and Options : The 510k Submission
GlobalCompliance Panel
1.5K views • 7 years ago
1:18:50
Statistical Concepts of Process Validation
GlobalCompliance Panel
18K views • 7 years ago
1:12:06
Medical Devices - ISO 14971 : Risk Management
GlobalCompliance Panel
28K views • 7 years ago
1:06:19
What to do during recalls, removals, and market corrections
GlobalCompliance Panel
935 views • 7 years ago
1:11:27
Purchasing and Supplier Controls in the Medical Device Industry
GlobalCompliance Panel
1.5K views • 7 years ago
1:08:12
Protocols for Medical Devices & Process Validation Principles
GlobalCompliance Panel
5.6K views • 7 years ago
1:28:00
Process Validation Procedure for Medical Device Manufacturers
GlobalCompliance Panel
6.9K views • 7 years ago
1:17:22
Outsourced processes and ISO 9001:2008
GlobalCompliance Panel
713 views • 7 years ago
59:53
Medical Device Design Control
GlobalCompliance Panel
12K views • 7 years ago
1:09:52
Medical Device Complaint Handling Systems
GlobalCompliance Panel
2.2K views • 7 years ago
1:13:42
Medical Device Adverse Event Reporting in EU, US and Canada
GlobalCompliance Panel
3.9K views • 7 years ago
1:05:37
Managing the Medical Device Supply Chain
GlobalCompliance Panel
1.3K views • 7 years ago
1:08:18
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
GlobalCompliance Panel
2.5K views • 7 years ago
1:03:26
Ensure data integrity and subject safety in clinical research
GlobalCompliance Panel
1K views • 7 years ago
1:10:24
FDA Requirements for Device Labeling
GlobalCompliance Panel
3.1K views • 7 years ago
58:29
How to prepare for an FDA inspection
GlobalCompliance Panel
1.9K views • 7 years ago
1:24:27
Understand the FDA device regulations related to Excel spreadsheets
GlobalCompliance Panel
1.2K views • 7 years ago
1:05:08
Equipment Validation, Tracking, Calibration, and Preventive Maintenance
GlobalCompliance Panel
3.7K views • 7 years ago
51:33
How to Meet FDA QSR and ISO 13485 Requirements in a Relatively Paper-Free Manner
GlobalCompliance Panel
559 views • 7 years ago
1:09:32
Regulatory Documents Explained - DHF, DMR, DHR and TF
GlobalCompliance Panel
5.5K views • 7 years ago
59:20
FDA QSR Requirements for DMR & DHR
GlobalCompliance Panel
631 views • 7 years ago
1:17:36
Recalls, Corrections and Removals (Devices)
GlobalCompliance Panel
295 views • 7 years ago
1:17:15
Effective Audit Program for both internal and external Processes
GlobalCompliance Panel
1.7K views • 7 years ago
1:02:57
FDA Quality Systems Regulation Requirements - Regulatory Documents Explained
GlobalCompliance Panel
8K views • 7 years ago
1:16:37
cGMP for Medical Devices Including IVDs
GlobalCompliance Panel
1.6K views • 7 years ago
Load More