| 1 |
- |
ISO 13485: Internal Auditor Training |
3 days |
29-31 |
View
|
| 2 |
- |
Workshop in Indian MDR 2017 |
2 days |
31st & 01st feb |
View
|
| 3 |
- |
ISO 13485: 2016 Lead Auditor Training |
5 days |
20,21,25,26,27 |
View
|
| 4 |
- |
Awareness of Risk Management |
1 Day |
21 |
-
|
| 5 |
- |
1 day workshop on Pharmacovigilance & Materiovigilance- The Future of Integrated Safety Monitoring |
1 Day |
26 |
View
|
| 6 |
- |
ISO 13485: Internal Auditor Training |
3 days |
25,26,27 |
View
|
| 7 |
- |
EU MDR Quality & Regulatory Compliance Program |
2 days |
21,22 |
View
|
| 8 |
- |
ISO 14971 : 2019 - Risk management requirements for Medical Devices |
2 days |
18,19 |
View
|
| 9 |
- |
Training program on Biomedical Equipment Maintenance Certification Scheme |
1 Day |
24 |
-
|
| 10 |
- |
Workshop in Indian MDR 2017 |
2 days |
9,10 |
View
|
| 11 |
- |
ISO 13485 : 2016 Lead Auditor |
5 days |
12-16 |
View
|
| 12 |
- |
Accessible built Environment as per NBC & PBCS Standards |
2 Day |
28-29 |
View
|
| 13 |
- |
US FDA Regulatory Compliance Training Program for Medical Devices |
2 days |
24,25 |
View
|
| 14 |
- |
ISO 13485: Internal Auditor Training |
3 days |
19-21 |
View
|
| 15 |
- |
Certificate in Quality Assurance |
2.5 months |
6th- Sep 26th |
View
|
| 16 |
- |
Hands-on Training Program on Hemovigilance Practices |
1 Day |
18 |
View
|
| 17 |
- |
Testing & Calibration Laboratories as per ISO/IEC 17025:2017 |
2 days |
23,24 |
View
|
| 18 |
- |
ISO 14971 : 2019 - Risk management requirements for Medical Devices |
2 days |
17-18 |
View
|
| 19 |
- |
Workshop in Indian MDR 2017 |
2 days |
11-12 |
View
|
| 20 |
- |
US FDA Regulatory Compliance Training Program for Medical Devices |
2 days |
25-26 |
View
|
| 23 |
- |
Testing & Calibration Laboratories as per ISO/IEC 17025:2017 |
2 days |
15-16 |
View
|
| 24 |
- |
ISO 13485: Internal Auditor Training |
3 days |
25-27 |
View
|
| 25 |
- |
Advanced Training Program in Biovigilance and Safety Monitoring |
1 Day |
19 |
View
|
| 26 |
- |
EU MDR Quality & Regulatory Compliance Program |
2 days |
19-20 |
View
|
| 27 |
- |
Workshop in Indian MDR 2017 |
2 days |
24-25 |
View
|
| 28 |
- |
Training program on HEALTEXPROF |
1 Day |
24 |
View
|
| 29 |
- |
US FDA Regulatory Compliance Training Program for Medical Devices |
2 days |
10-11 |
View
|
| 30 |
- |
ISO 14971 : 2019 - Risk management requirements for Medical Devices |
2 days |
17-18 |
View
|
| 31 |
- |
Testing & Calibration Laboratories as per ISO/IEC 17025:2017 |
2 days |
21-22 |
View
|
| 32 |
- |
Certificate in Quality Assurance |
50 hours/ 3.5 Months |
7th- 15th Mar 2027 |
View
|
| 33 |
- |
ISO 13485: Internal Auditor Training |
3 days |
25-27 |
View
|
| 34 |
- |
EU MDR Quality & Regulatory Compliance Program |
2 days |
12-13 |
View
|
| 35 |
- |
ISO 13485 : 2016 Lead Auditor certification course |
5 days |
10-14 |
View
|