| 1 |
MEDICAL DEVICE ADVERSE EVENT REPORTING FORM Version 1.2 |
2024-Oct-08 |
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656 KB |
| 2 |
Draft Guidelines on Good Clinical Practices |
2024-Sep-12 |
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3315 KB |
| 3 |
Baxter recall letter for Product Fibrin Sealant Kit Brand name Tisseel Lyo manufactured in Vienna Austria |
2024-Sep-02 |
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1508 KB |
| 4 |
Details of Rejected clinical trial applications / permissions (Form CT-04 and CT-06) 2024 |
2024-Aug-30 |
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8 KB |
| 5 |
Details of clinical trial Permissions of Year 2024 |
2024-Aug-30 |
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196 KB |
| 6 |
Approved panel of experts for the Subject Expert Committees |
2024-Aug-29 |
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493 KB |
| 7 |
Appointment of CPIO for the purpose of RTI Technical Matters 7 Aug 24 |
2024-Aug-07 |
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96 KB |
| 8 |
Names of countries under the Rule 101 of New Drugs and Clinical Trial Rules 2019 related to new drug approval |
2024-Aug-07 |
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280 KB |
| 9 |
Surrender of Cosmetics Import Registration Certificates of M/s Johnson & Johnson Pvt. Ltd L.B.S. Marg Mulund Mumbai Maharashtra India |
2024-Aug-06 |
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997 KB |
| 10 |
PRO feedback form Internal and Pro feedback form External |
2024-Jul-26 |
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909 KB |
