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Drugs
Sale Licenses
Fee for sale licenses
Sale Licenses – Drug and Homoeopathic
Jan Aushadhi Store (PMBJP)
Record keeping for Medical Store / Pharmacy
Pharmacist Change at Medical Store
Self inspection of Medical Store
Good storage practice of Medicines at Medical Store
Medical Devices: Registration for sale
Manufacturing Licenses
Fee for manufacturing licenses
Area required for manufacturing
Schedule M
Revised Schedule M
Key Notes on Revised Schedule M: Compilation
WHO TRS 1044 Annex 2
Allopathic Drugs
Allopathic Drugs – Repacking
Cosmetics – Manufacturing License
Homoeopathic – Manufacturing License
Medical Device
Fee for Medical Devices
Medical Devices – Manufacturing License
Classifications of Medical Devices
Notified Bodies for Medical Devices
Medical Devices Policy 2023
Manufacturing of drugs for testing and analysis
LVP, Sera & Vaccines – Manufacturing License
Blood Products
Blood Bank / Centre
Blood Bank / Centre
Blood Donation Camp
Blood Storage Centre
Bulk transfer of Blood and Blood Components: Procedure and Conditions
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 (NDPS)
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
Committee
DCC
DTAB
Technical Committee
Hathi Committee
Mashelkar Committee
Forms
Forms: Drugs
Forms: for Cosmetics
Forms: For Homoeopathy Medicine
Forms: for Medical Devices
Forms: Clinical Trial
Forms: for Hospital RMI
Fee
Schedules
Schedules: for Drugs
Schedule M
Schedules: for Cosmetics
Schedules: for Medical Devices
Schedules: for Clinical Trials
Alert
Drug Alert: NSQ Drugs Lists
Medical Device Alert: Lists
IPC Alert
WHO Alert
Govt Job Alert
Drug recall
Medical Device recall
Legal
Legislations: India
Notifications
Banned Drugs: Notifications
Blood Bank / Centre – Notifications
Cosmetics – Notifications
COTPA – Notifications
DMR(OA) Notifications
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
NPPA – DPCO: Notifications & News
Testing Laboratories – Notifications
Articles
Articles -Legal
Articles -Pharma & Cosmetics
Important short notes for Industry and Regulators
Key Notes on Revised Schedule M: Compilation
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Home
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GMP
Tag: GMP
Industry
USFDA issues EIR For Piramal Pharma Bethlehem Facility
The Health Master
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November 10, 2023
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Industry
USFDA issued OAI Status to Biocon Subsidiary
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October 18, 2023
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Industry
Pharmaceutical Quality: Key Amendments in Revised Schedule M
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October 17, 2023
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Industry
October 10: National GMP Day – A Turning Point
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October 9, 2023
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Industry
Revised Schedule M: Govt sets deadline for pharma industry
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October 2, 2023
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Industry
Major cracks down on Pharma MSMEs for gross GMP violations
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August 29, 2023
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Industry
Pharma Industry Gears Up for Revised Schedule M: Gujarat
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August 28, 2023
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Industry
Gujarat FDCA takes stringent actions against Non-Compliant Pharma Companies
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August 5, 2023
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Govt to implement GMP for Pharma Companies to enhance quality and global acceptance
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August 2, 2023
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Industry
USFDA issues warning letter to Torrent Pharma for Gujarat facility
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January 24, 2023
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Industry
USFDA issues warning letter to Sun Pharma for its Gujarat plant
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January 14, 2023
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Nation
There is need for clear definition of excipients and its GMP: IPEC
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November 3, 2021
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Nation
Virtual workshops series to be organized on GMP
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July 24, 2021
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Industry
Merck launches synthetic cholesterol product
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May 29, 2021
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World
India to Arab Countries: To make Pharma Export easier
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February 25, 2021
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Gujarat FDCA to give boost to MSMEs
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January 28, 2021
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World
USFDA, Gujarat FDCA officials share experiences of pandemic
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January 21, 2021
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Wallace Pharma sets up R&D Centre in Goa
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January 2, 2021
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PLI scheme: GMP is key for domestic APIs
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December 9, 2020
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World
CDSCO, UK MHRA to sign MoU on regulation of medicines, medical devices
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November 5, 2020
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Industry
USFDA’s inspection of Biocon with 5 observations
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January 29, 2020
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Draft guidelines finalized on post-approval changes in drugs
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January 14, 2020
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World
Indian and global regulatory systems
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December 24, 2019
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Authors
Rakesh Dahiya
139 POSTS
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Nidhi Gudwani
40 POSTS
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Lalit Kr. Goel
40 POSTS
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N K Ahooja
20 POSTS
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Dr. Kumud Madan
13 POSTS
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Dipika Chauhan
13 POSTS
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Naripen Goyal
11 POSTS
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Sushant Mahapatra
9 POSTS
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Dr. Bharatesh R Jagashetty
7 POSTS
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Dr. B Suresh
5 POSTS
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Manmohan Taneja
5 POSTS
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Dr. J K Jha
5 POSTS
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Dr. BN Nagpal
4 POSTS
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Dr. Brahmdeep Sindhu
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H. Mahapatra
3 POSTS
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Nilesh Gandhi
3 POSTS
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http://www.pharmastute.com
Dr. P K Sreekumar
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Dr. NPS Verma
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P K Jaggi
1 POSTS
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Sanjay Malhotra
1 POSTS
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http://www.aerolgroup.com
P P Sharma
1 POSTS
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Dr. Balraj Yadav
1 POSTS
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Dr. Gulshan Rai Arora
1 POSTS
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Prof Vivek Padgaonkar
1 POSTS
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https://www.linkedin.com/in/vivek-padgaonkar-8298509/
Adarsh Goyal
1 POSTS
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K C Aggarwal
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