Channel Avatar

Patient Guard Limited @UCyh3YzixtKlvK_M6--lQmqA@youtube.com

388 subscribers - no pronouns :c

Patient Guard is a Medical Device Regulatory Affairs and Qua

Videos Playlists
Recently Uploaded Popular Oldest
04:40
Risk Management of Medical Devices and IVDs | Patient Guard
04:35
Medical Device and IVD Technical Files | Patient Guard
05:29
Understanding the Role of the PRRC for Medical Devices and IVDs in the EU | Patient Guard
04:12
EU Authorised Representative PPE | Patient Guard
03:52
EU Representative for Cosmetics | Patient Guard
06:07
EU Authorised Representative | Patient Guard
05:08
Personal Protective Equipment (PPE) Regulations | Patient Guard
03:43
UKRP for Cosmetics | Patient guard
04:33
UK Responsible Person (UKRP) – Medical Devices | Patient Guard
02:22
The Biological Evaluation of Medical Devices | Patient Guard
03:24
Understanding Cytotoxicity Testing | Patient Guard
04:10
In Vitro Skin Irritation Testing: ISO 10993-23 Standard | Patient Guard
04:03
Drug Stability in Medical Devices | Patient Guard
07:43
Extractables and Leachables Testing for Medical Devices in ISO 10993 | Patient Guard
05:18
Understanding the core elements of Quality Management Systems | Patient Guard
04:21
5 Differences Between ISO 13485 & FDAs Medical Device QSR | | Patient Guard
08:01
Mastering Medical Device Standards: The Essential Guide for All Device Types
01:40
Wearable Medical Devices Transforming Healthcare
07:19
ISO 14971 and the risk management of medical devices
02:47
IEC 62366 1 Usability Engineering for Medical Devices
03:36
The sterilisation of medical devices and the methods used
03:35
Medical Device Labelling - ISO 15223 Medical Symbols
04:23
The Electrical Safety of Medical Devices
04:44
Clinical Evaluation of Medical Devices
01:47
Regulating AI (Artificial Intelligence) Medical Devices
02:42
Identifying if a product is an IVD under EU IVDR 2017/746
04:08
Navigating EU Regulations: Is My Product a Medical Device?
02:30
FDA Medical Device Classification
03:12
Classification of Medical Devices - EU 2017/745
01:59
A History of Medical Device Regulation - FDA
01:48
A History of Medical Devices from ancient times to the present day
01:27
Exploring Medical Device UDI (Unique Device Identification)
01:28
Medical Devices - An Introduction to the EU EUDAMED system
02:03
Software as a Medical Device (SaMD) and how it is regulated in the EU
01:54
Understanding Medical Device Biological Evaluation - Biological Evaluation Report ISO 10993-1
02:22
Biological Evaluation Plan (BEP) - Medical Devices (ISO 10993)
04:36
The Biological Evaluation of Medical Devices
01:38
EU Authorised Representative Role - Medical Devices
01:34
Medical Devices - UK Responsible Person Role
02:43
The UK vs the EU Medical Device Regulations - What are the key differences?
02:04
Understanding PRRC (Person Responsible for Regulatory Compliance) under EU MDR & IVDR Regulations
02:19
Understanding the FDA Medical Device 510k Process
02:11
Patient Guard Introduction Video
02:09
Medical Device UKCA marking
01:53
CE Marking for Medical Devices: Ensuring Safety and Compliance
05:14
In Vitro Diagnostic Regulations EU 2017/746 - What are they?
04:07
Navigating the EU Medical Device Regulation 2017/745
03:28
How are ISO 13485 and ISO 14971 linked?
04:32
Understanding Quality Management Systems - ISO 13485 - Clause 8.5 - Improvement
04:36
Understanding Quality Management Systems - ISO 13485 - Clause 8.4 - Analysis of Data
04:47
Understanding Quality Management Systems -ISO 13485 - Clause 8.3 - Control of Non-conforming Product
02:03
ISO 10993 part 1 - Biocompatibility of Medical Devices
02:47
Understanding Quality Management Systems ISO 13485-Cause 8.2.6-Monitoring & Measurement of Product
02:56
The Risk Management of Medical Devices - ISO 14971
03:11
Understanding Quality Management Systems -ISO 13485 - 8.2.5 - Monitoring & Measurement of Processes
03:08
Understanding Quality Management Systems - ISO 13485 - Clause 8.2.4 - Internal Audits
04:42
Shocking Medical Device scandals and why global Medical Device regulation became stricter.
02:52
Understanding Quality Management Systems ISO 13485 Clause 8.2.3 reporting to regulatory authorities
03:18
Understanding Quality Management Systems - ISO 13485 - Clause 8.2.2 - Complaint Handling
02:53
What the difference between ISO 9001 and ISO 13485?
Next Page