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CDSCO & ICH Guidelines on Packaging for Stability Testing
Pharmaceutical packaging: not just a container, but a vital protector. It's the silent guardian ensuring your medicine remains safe,...
Akshay Gautam
Aug 30, 20258 min read


Tariffs, Trade & Triumph: The Indian Pharma Response to Trump’s Policies
From tariff shocks to “Buy American” pressures, Trump’s policies tested Indian pharma’s resilience. Yet, in the world’s largest drug...
Akshay Gautam
Aug 23, 202512 min read


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


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


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


GMP Series (Schedule M): 1.3 Water system
In the pharmaceutical manufacturing, the quality of every component is paramount to ensure the safety and efficacy of the final products....
Jyotsna Sharma
Oct 17, 202312 min read


GLP Series (Schedule L): 3 Personnel
Personnel standards are vital in pharmaceutical laboratories, with qualifications, training, and experience ensuring data integrity. The...
Ashima Thakur
Oct 17, 202313 min read


GLP Series (Schedule L): 2 Premises
Here is the essential criteria for upholding quality and safety within laboratory premises. These criteria encompass measures to prevent...
Ashima Thakur
Oct 15, 202314 min read
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