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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
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Important short notes for Industry and Regulators
Key Notes on Revised Schedule M: Compilation
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WHO GMP
Tag: WHO GMP
Industry
Govt boosts Pharma Companies with Revamped Scheme
The Health Master
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August 11, 2024
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Industry
DCGI announces Stringent Measures and Digital Transformation Plans
The Health Master
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June 29, 2024
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Industry
Gujarat FDCA Equips Pharma Industry for Revised Schedule M
The Health Master
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June 17, 2024
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Industry
Gujarat FDCA and IDMA Join Forces for GMP Compliance Training
The Health Master
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May 20, 2024
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Industry
Indian Pharma Industry Gears Up to comply Revised Schedule M
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May 18, 2024
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Industry
USFDA Inspection: At Strides Pharma with 2 observations
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April 10, 2024
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Nation
Venus Remedies gets GMP certificate from Libya: A Gateway to African Markets
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January 25, 2024
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Industry
Challenges Faced by MSME Pharma Industries on Revised Schedule M
The Health Master
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January 11, 2024
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Industry
Gist of 31 Chapters on Schedule M
Lalit Kr. Goel
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November 22, 2023
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Nation
Revised Schedule M Guidelines: Drug Recall and Ensuring Pharma Quality
The Health Master
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November 20, 2023
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Industry
USFDA issues EIR For Piramal Pharma Bethlehem Facility
The Health Master
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November 10, 2023
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Industry
Revised Schedule M: Govt sets deadline for pharma industry
The Health Master
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October 2, 2023
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Industry
Govt to roll out schemes for strengthening Pharma Industry
The Health Master
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July 20, 2022
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Nation
Govt to implement PTUA scheme soon for Pharma MSMEs
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November 16, 2021
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Industry
Lincoln Pharma plans to launch Cephalosporin products
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September 22, 2021
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World
Gujarat FDCA to host meet with USFDA for information sharing
The Health Master
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March 21, 2021
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States
Gujarat FDCA introduces online facility for WHO-GMP certification with QR Code
The Health Master
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March 1, 2021
0
States
5 lakhs Product Permissions, 4,880 Mfg Licences issued: Gujarat FDCA
The Health Master
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March 1, 2021
0
States
Gujarat FDCA to give boost to MSMEs
The Health Master
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January 28, 2021
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World
USFDA, Gujarat FDCA officials share experiences of pandemic
The Health Master
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January 21, 2021
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Authors
Rakesh Dahiya
138 POSTS
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Lalit Kr. Goel
40 POSTS
0 COMMENTS
Nidhi Gudwani
40 POSTS
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N K Ahooja
20 POSTS
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Dipika Chauhan
13 POSTS
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Dr. Kumud Madan
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. J K Jha
5 POSTS
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Dr. B Suresh
5 POSTS
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Manmohan Taneja
5 POSTS
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Dr. Brahmdeep Sindhu
4 POSTS
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Dr. BN Nagpal
4 POSTS
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Nilesh Gandhi
3 POSTS
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http://www.pharmastute.com
H. Mahapatra
3 POSTS
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Dr. NPS Verma
2 POSTS
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Dr. P K Sreekumar
2 POSTS
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K C Aggarwal
1 POSTS
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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
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