Device Master Record & Device History Record - A Regulatory

  Рет қаралды 1,841

GlobalCompliance Panel

GlobalCompliance Panel

Күн бұрын

Пікірлер: 1
@benlee3545
@benlee3545 Жыл бұрын
hi, your video is good. you also share some of the experience you have in software but it will be better if you can include examples of the device master record for clearer illustrations and templates etc.
Managing the Medical Device Supply Chain
1:05:37
GlobalCompliance Panel
Рет қаралды 1,5 М.
FDA Requirements for Device Labeling
1:10:24
GlobalCompliance Panel
Рет қаралды 3,4 М.
Mom Hack for Cooking Solo with a Little One! 🍳👶
00:15
5-Minute Crafts HOUSE
Рет қаралды 23 МЛН
Каха и дочка
00:28
К-Media
Рет қаралды 3,4 МЛН
小丑教训坏蛋 #小丑 #天使 #shorts
00:49
好人小丑
Рет қаралды 54 МЛН
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
1:08:18
Purchasing and Supplier Controls in the Medical Device Industry
1:11:27
GlobalCompliance Panel
Рет қаралды 1,5 М.
Medical Devices - ISO 14971 : Risk Management
1:12:06
GlobalCompliance Panel
Рет қаралды 28 М.
Requirements Contents and Options : The 510k Submission
1:19:59
GlobalCompliance Panel
Рет қаралды 1,7 М.
What to do during recalls, removals, and market corrections
1:06:19
GlobalCompliance Panel
Рет қаралды 991
Process Validation Procedure for Medical Device Manufacturers
1:28:00
GlobalCompliance Panel
Рет қаралды 7 М.
Medical Device Complaint Handling Systems
1:09:52
GlobalCompliance Panel
Рет қаралды 2,5 М.
Understanding Attribute Acceptance Sampling including Z1 4 and c=0 Plans
1:29:36
GlobalCompliance Panel
Рет қаралды 12 М.
Medical Device Adverse Event Reporting in EU, US and Canada
1:13:42
GlobalCompliance Panel
Рет қаралды 4,1 М.
Ensure data integrity and subject safety in clinical research
1:03:26
GlobalCompliance Panel
Рет қаралды 1 М.
Mom Hack for Cooking Solo with a Little One! 🍳👶
00:15
5-Minute Crafts HOUSE
Рет қаралды 23 МЛН