Custom-Made Device Manufacturer Requirements under MDR
13:09
Custom-Made Device Manufacturer Requirements under MDR
5 ай бұрын
Custom-Made Devices - demonstrating regulatory compliance
30:03
Custom-Made Devices - demonstrating regulatory compliance
5 ай бұрын
Complaints and Reporting to the Competent Authority - Post-Market Surveillance and Vigilance
19:04
Complaints and Reporting to the Competent Authority - Post-Market Surveillance and Vigilance
5 ай бұрын
Questions and Answers session
20:31
Questions and Answers session
5 ай бұрын
In Vitro Diagnostic Medical Devices Regulation - in house IVD’s
51:01
In Vitro Diagnostic Medical Devices Regulation - in house IVD’s
6 ай бұрын
Ní chreidfidh tú cad a sheol siad dom!!
0:15
Ní chreidfidh tú cad a sheol siad dom!!
Жыл бұрын
How to report an adverse event using the online reporting form
15:20
How to report an adverse event using the online reporting form
Жыл бұрын
The role of animal owners in monitoring the safety and effectiveness of veterinary medicines
14:37
The role of animal owners in monitoring the safety and effectiveness of veterinary medicines
Жыл бұрын
Adverse event reporting for vets, vet nurses and animal healthcare professionals
24:16
Adverse event reporting for vets, vet nurses and animal healthcare professionals
Жыл бұрын
I got sicker!
0:15
I got sicker!
Жыл бұрын
You won't believe what they sent me
0:15
You won't believe what they sent me
Жыл бұрын
Cleaning Validation
21:40
Cleaning Validation
2 жыл бұрын
Registration requirements and certificates of free sale
19:59
Registration requirements and certificates of free sale
2 жыл бұрын
Performance studies
24:17
Performance studies
2 жыл бұрын
HPRA IVD inspection activities
22:57
HPRA IVD inspection activities
2 жыл бұрын
Post - market surveillance, vigilance and market surveillance
24:38
Post - market surveillance, vigilance and market surveillance
2 жыл бұрын
European and national implementation of the IVDR
31:06
European and national implementation of the IVDR
2 жыл бұрын
Annex 21 - Importation of medicinal products
22:18
Annex 21 - Importation of medicinal products
2 жыл бұрын
Out-of-specification (OOS) investigations
27:04
Out-of-specification (OOS) investigations
2 жыл бұрын
Management of outsourced activities and QP responsibilities
23:07
Management of outsourced activities and QP responsibilities
2 жыл бұрын
HPRA quality defects and recall (QDR) programme
30:08
HPRA quality defects and recall (QDR) programme
2 жыл бұрын
Overview of GMP inspections, 2018 2021
31:47
Overview of GMP inspections, 2018 2021
2 жыл бұрын
Key updates of interest
19:41
Key updates of interest
2 жыл бұрын
Safety features update
20:37
Safety features update
2 жыл бұрын
Deficiency trending
19:16
Deficiency trending
2 жыл бұрын
Temperature mapping
20:08
Temperature mapping
2 жыл бұрын
Transport and outsourced activities
16:22
Transport and outsourced activities
2 жыл бұрын
Clinical Trial Regulation: Post-authorisation, transition and how can I prepare
1:00:06
Clinical Trial Regulation: Post-authorisation, transition and how can I prepare
2 жыл бұрын
How we will implement the Clinical Trial Regulation in Ireland
1:02:37
How we will implement the Clinical Trial Regulation in Ireland
2 жыл бұрын
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