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Mandatory CDSCO Guidelines For Labeling Compliance in India
Ensuring every pharmaceutical label meets CDSCO’s strict standards isn’t optional; it’s the key to patient safety, regulatory approval,...
Akshay Gautam
Aug 16, 20256 min read


CDSCO VS State FDA: Approval Authority in India
Navigate the distinct roles of CDSCO and State FDA to ensure faster approvals, full compliance, and successful market entry. 1....
Akshay Gautam
Aug 8, 202510 min read


How the India–UK FTA Opens New Doors for Indian Pharma & CDMOs
The India-UK Free Trade Agreement unlocks zero-duty access and faster approvals for Indian pharma exports, paving the way for deeper...
Akshay Gautam
Aug 2, 202511 min read


Pharma Opportunities Ahead: Key Drugs Going Off-Patent in India (2025-2027)
Explore high-impact opportunities as branded and blockbuster drugs lose patent protection in India between 2025-2027. Gain insights into...
Akshay Gautam
Jul 26, 202511 min read


Understanding NDCTR 2019: A Key Guide for Pharma Manufacturers and Marketers Launching Products in India
India’s New Drugs and Clinical Trials Rules, 2019, mark a significant regulatory shift offering pharmaceutical companies streamlined...
Akshay Gautam
Jul 19, 20257 min read


If It’s Not a CDSCO-Approved Drug, It’s Not Legal. Don’t Risk Your Pharma Brand
Don’t be fooled by “approved” products without regulatory backing. Your responsibility as a marketer or a pharmaceutical company starts...
Akshay Gautam
Jul 14, 20257 min read


Film Coating Process in Pharmaceutical Manufacturing
For pharmaceutical companies seeking reliable third-party manufacturing, the film coating process is a critical step that enhances the...
The Walter Way
Jul 8, 20256 min read


An Informative Guide to the Hardness of Tablets
Discover the complexities behind pharmaceutical tablet development, from formulation to manufacturing, as we explore the scientific,...
Marketing - Walter®
Jul 3, 20255 min read


The Science of Drug Stability
How to ensure long-lasting efficacy Did you know that even the most effective drug can fail if it's not stored properly? Stability is a...
The Walter Way
Jun 7, 20256 min read


GLP Series (Schedule L): 13. Standard Operating Procedure
Standard Operating Procedures (SOPs) are crucial documents in laboratory settings, providing detailed instructions on how to conduct...
Marketing - Walter®
Apr 16, 20242 min read


Vitamin B1: Essential Nutrient for Energy and Well-Being
Introduction Vitamin B1, also known as thiamine, is an essential nutrient that helps the body convert food into energy. Thiamine plays a...
Marketing - Walter®
Mar 20, 20243 min read


GLP Series (Schedule L): 11 Internal Quality System Audits
In the intricate landscape of laboratory operations, maintaining the highest standards of quality is paramount. Internal quality system...
Marketing - Walter®
Feb 8, 20242 min read


GLP Series (Schedule L): 9 Microbiological Cultures
Microbial cultures are vital in scientific research, especially in pharmaceuticals and biotech. Effective management through maintenance,...
Ashima Thakur
Dec 2, 202313 min read


GLP Series (Schedule L): 8 Reference Materials
Lab guidelines emphasize using traceable reference materials, precise preparation of standards, unique coding, and detailed registers....
Ashima Thakur
Dec 2, 202312 min read


GMP Series (Schedule M): 6. Personnel
Ensuring the integrity and excellence of pharmaceutical manufacturing: A comprehensive guide to personnel criteria in maintaining...
Jyotsna Sharma
Nov 23, 202312 min read


GMP Series (Schedule M): 5. Quality Control area
Quality control is a critical aspect of any manufacturing or production process, ensuring that products meet the required standards and...
Jyotsna Sharma
Nov 18, 202312 min read


GLP Series (Schedule L): 7 Maintenance, Calibration, and Validation of Equipments
Equipment maintenance and calibration are top priorities to ensure precision and reliability in laboratory operations, demonstrating...
Ashima Thakur
Nov 18, 202312 min read


GMP Series (Schedule M): 4. Ancillary Areas
In pharmaceutical manufacturing, strict rules enforce the separation of ancillary areas from restrooms, maintenance zones, and animal...
Jyotsna Sharma
Nov 5, 202312 min read


GMP Series (Schedule M): 3 Production area
The production area in the pharmaceutical sector is the designated space where medicines and drugs are manufactured, and it is of...
Jyotsna Sharma
Nov 5, 20232 min read


GLP Series (Schedule L): 6 Good House Keeping and Safety
Laboratory safety is paramount and entails providing safety instructions, adhering to regulatory SOPs, and implementing protective...
Ashima Thakur
Nov 4, 202313 min read


GLP Series (Schedule L): 5 Chemicals and Reagents
Proper management of chemicals in a laboratory is essential for safety and reliable research. This involves safe storage, labeling,...
Ashima Thakur
Nov 4, 202313 min read


GLP Series (Schedule L): 4 Equipments
Equipment maintenance in Good Laboratory Practices (GLP) is important for pharmaceutical manufacturing, covering equipment readiness,...
Ashima Thakur
Nov 4, 202313 min read


GMP Series (Schedule M): 2 Warehousing Area
Following essential guidelines and practices in a warehouse ensures safe storage, orderly organization, and quality assurance for diverse...
Jyotsna Sharma
Nov 4, 202313 min read


GMP Series (Schedule M): 1.4 Disposal of waste
In pharmaceutical sector, where innovation and quality take center stage, it's crucial for companies to not only focus on producing...
Jyotsna Sharma
Oct 19, 202312 min read
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