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Manufacturing License
Fee for manufacturing licenses
Area required for manufacturing
Schedule M
Revised Schedule M
Key Notes on Revised Schedule M: Must read
WHO TRS 1044 Annex 2
Allopathic Drugs
Allopathic Drugs – Repacking
Cosmetics – Manufacturing License
Homoeopathic – Manufacturing License
Medical Devices
Fee for Medical Devices
Medical Devices – Manufacturing License
Classifications of Medical Devices
Notified Bodies for Medical Devices
Medical Device Policy 2023
Manufacturing of drugs for testing and analysis
LVP, Sera & Vaccines – Manufacturing License
Blood Products
Blood Bank / Centre
Fee for Blood centre
Area required for Blood centre
Blood Bank / Centre
Blood Storage Centre
Blood Donation Camp
Bulk transfer of Blood and Blood Components: Procedure and Conditions
Pharmacopoeial status of Blood and its components
Testing Laboratories
Govt Laboratories: Updates
Commercial Testing Laboratories: Procedure
Medical Device Testing Laboratories (MDTLs): Procedure
NABL for Laboratories
List of Laboratory instruments for testing
Calibration of Laboratory Instruments
Hospital – RMI
Banned Drugs
Drug Dosage as per IP
Storage conditions of drugs
Light sensitive drugs / medicines: List
Import of Drugs
National Pharmaceutical Pricing Authority (NPPA)
Indian Pharmacopoeia Commission (IPC)
National Formulary of India (NFI)
National List of Essential Medicines (NLEM)
New Drugs, FDCs, Clinical trial
BA / BE Studies
Nutraceuticals
Nanopharmaceuticals
Phytopharmaceuticals
Committees
DCC
DTAB
Technical Committee
Hathi Committee
Mashelkar Committee
Forms
Forms: Drugs
Forms: for Cosmetics
Forms: for Medical Devices
Forms: Clinical Trial
Fee
Schedules
Schedules: for Drugs
Schedule M
Schedules: for Cosmetics
Schedules: for Medical Devices
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Alert
Drug Alert: NSQ Drugs Lists
Medical Device Alert: Lists
IPC Alert
WHO Alert
Govt Job Alert
Drug recall
Legal
Legislations: India
Notifications
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Blood Bank / Centre – Notifications
Cosmetics – Notifications
COTPA – Notifications
DMR(OA)
Drugs Act – Notifications
Drug Rules – Notifications
EC Act – Notifications
General – Notifications
Homoeopathic – Notifications
Hospital – RMI: Notifications
Medical Devices – Notifications
NDPS Act – Notifications
New Drugs, FDC, Clinical Trial – Notifications
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CGMP
Tag: cGMP
Industry
USFDA issued Form 483 with 5 observations to Alembic
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November 25, 2024
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June 27, 2024
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June 22, 2024
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June 20, 2024
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CDSCO underscores stringent compliance to Revised Schedule M
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Page 1 of 2
Authors
Rakesh Dahiya
127 POSTS
0 COMMENTS
Lalit Kr. Goel
40 POSTS
0 COMMENTS
Nidhi Gudwani
40 POSTS
0 COMMENTS
N K Ahooja
20 POSTS
0 COMMENTS
Dipika Chauhan
13 POSTS
0 COMMENTS
Dr. Kumud Madan
13 POSTS
0 COMMENTS
Naripen Goyal
11 POSTS
0 COMMENTS
Sushant Mahapatra
9 POSTS
0 COMMENTS
Dr. Bharatesh R Jagashetty
7 POSTS
0 COMMENTS
Manmohan Taneja
5 POSTS
0 COMMENTS
Dr. J K Jha
5 POSTS
0 COMMENTS
Dr. B Suresh
5 POSTS
0 COMMENTS
Dr. Brahmdeep Sindhu
4 POSTS
0 COMMENTS
Dr. BN Nagpal
4 POSTS
0 COMMENTS
Nilesh Gandhi
3 POSTS
0 COMMENTS
http://www.pharmastute.com
H. Mahapatra
3 POSTS
0 COMMENTS
Dr. NPS Verma
2 POSTS
0 COMMENTS
Dr. P K Sreekumar
2 POSTS
0 COMMENTS
Dr. Gulshan Rai Arora
1 POSTS
0 COMMENTS
Prof Vivek Padgaonkar
1 POSTS
0 COMMENTS
https://www.linkedin.com/in/vivek-padgaonkar-8298509/
Adarsh Goyal
1 POSTS
0 COMMENTS
K C Aggarwal
1 POSTS
0 COMMENTS
P K Jaggi
1 POSTS
0 COMMENTS
Sanjay Malhotra
1 POSTS
0 COMMENTS
http://www.aerolgroup.com
P P Sharma
1 POSTS
0 COMMENTS
Dr. Balraj Yadav
1 POSTS
0 COMMENTS