|
Medical Device
|
| 01 |
Biologics/Biosimilar Submission as per US and EU |
10 Days |
7500 |
Apply Now |
| 02 |
Medical Device labeling as per EU and ISO 15223 |
10 Days |
3500 |
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| 03 |
Pharmaceutical Product labeling as US, EU and India |
10 Days |
3500 |
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| 04 |
Computer System Validation, 21 CFR part 11, GAMP 5 |
10 Days |
7500 |
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| 05 |
Internal Auditor/Lead Auditor QMS 13485-2016, ISO 19011-2018 Course |
10 Days |
7500 |
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| 06 |
Medical Device -Indian Regulation, BIS Submission, Sugam Portal Submission |
1 week |
3500 |
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| 07 |
Medical Device-European MDR, CE Mark |
1 week |
3500 |
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| 08 |
Medical Device- USFDA Submission |
1 week |
3500 |
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| 09 |
MDD to MDR Implementation |
1 week |
3500 |
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| 10 |
Medical Device-Risk Management |
1 week |
3500 |
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| 11 |
Medical Device Design and Development |
1 week |
3500 |
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|
Pharmaceutical
|
| 12 |
Effective CMC Writing and Review Skills |
1 week |
7500 |
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| 13 |
Drug Regulation In US |
1 week |
2500 |
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| 14 |
Drug Regulation in Europe |
1 week |
2500 |
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| 15 |
Drug Regulation in ROW |
1 week |
2500 |
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| 16 |
Drug Substance Regulation-Drug Master File |
1 week |
2500 |
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| 17 |
Formulation Development |
1 week |
1500 |
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| 18 |
Drug Development Process |
1 week |
1500 |
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| 19 |
Good Manufacturing Practice |
1 week |
1500 |
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| 20 |
Regulatory System in Canada |
1 week |
1500 |
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| 21 |
ICH Q 1-Stability Studies |
1 week |
1500 |
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| 22 |
ICH Q2-Analytical Validation |
1 week |
1500 |
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| 23 |
ICH Q3-Impurities |
1 week |
1500 |
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| 24 |
ICH Q 6-Specification |
1 week |
1500 |
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| 25 |
ICH Q9- Quality Risk Management |
1 week |
1500 |
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| 26 |
ICH Q10- Pharmaceutical Quality Management |
1 week |
1500 |
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| 27 |
Importance of Data Integrity in Pharmaceuticals |
1 week |
1500 |
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|
NUTRACEUTICALS
|
| 28 |
Regulatory Perspective of Nutraceuticals |
1 week |
1500 |
Apply Now |