Patient Guard Limited
Patient Guard is a Medical Device Regulatory Affairs and Quality Assurance Service Business. We help Medical Device & In Vitro Diagnostic (IVD) Device manufacturers, distributors and other stakeholders remain compliant with the Medical Device Regulations.Our Medical Device & IVD experts can assist with EU & UK Medica Device Regulation and Quality Assurance Requirements.
Our videos aim to be an educational tool for people wanting to learn more about Medical Devices & IVDs. As well as Medical Device Consultancy, we also sell templates to help professionals in the Medical Device sector with their compliance needs.
What ever your Medical Device compliance needs we will be happy to help.
- 7:19
- 3 ай бұрын
ISO 14971 and the risk management of medical devices
- 2:47
- 3 ай бұрын
IEC 62366 1 Usability Engineering for Medical Devices
- 3:35
- 4 ай бұрын
Medical Device Labelling - ISO 15223 Medical Symbols
- 4:23
- 4 ай бұрын
The Electrical Safety of Medical Devices
- 4:44
- 4 ай бұрын
Clinical Evaluation of Medical Devices
- 1:47
- 4 ай бұрын
Regulating AI (Artificial Intelligence) Medical Devices
- 2:30
- 5 ай бұрын
FDA Medical Device Classification
- 3:12
- 5 ай бұрын
Classification of Medical Devices - EU 2017/745
- 1:59
- 6 ай бұрын
A History of Medical Device Regulation - FDA
- 1:54
- 7 ай бұрын
Understanding Medical Device Biological Evaluation - Biological Evaluation Report ISO 10993-1
- 4:36
- 8 ай бұрын
The Biological Evaluation of Medical Devices
- 1:38
- 8 ай бұрын
EU Authorised Representative Role - Medical Devices
- 1:34
- 8 ай бұрын
Medical Devices - UK Responsible Person Role
- 2:04
- 8 ай бұрын
Understanding PRRC (Person Responsible for Regulatory Compliance) under EU MDR & IVDR Regulat...
- 2:19
- 9 ай бұрын
Understanding the FDA Medical Device 510k Process
- 2:11
- 9 ай бұрын
Patient Guard Introduction Video
- 2:09
- 9 ай бұрын
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