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Ashima Thakur
Dec 2, 202313 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,...
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Ashima Thakur
Dec 2, 202312 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....
34 views
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Jyotsna Sharma
Nov 23, 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...
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Jyotsna Sharma
Nov 18, 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...
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Jyotsna Sharma
Nov 5, 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...
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Jyotsna Sharma
Nov 5, 20232 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...
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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,...
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Jyotsna Sharma
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...
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Jyotsna Sharma
Oct 19, 202312 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...
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Jyotsna Sharma
Oct 17, 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....
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Ashima Thakur
Oct 15, 202314 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...
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Jyotsna Sharma
Sep 26, 202313 min read
GMP Series (Schedule M): 1.1 Location and Surroundings
Location and surroundings are critical considerations in the pharmaceutical sector, influencing factors such as regulatory compliance,...
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Jyotsna Sharma
Sep 16, 202314 min read
The Pillars of Quality: A Deep Dive into Process Validation at Walter®
Process validation in the pharmaceutical sector is a critical and regulated activity that ensures that a pharmaceutical manufacturing...
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Ashima Thakur
Jul 25, 202312 min read
Pharma ISO Certifications: Driving Excellence & Compliance
ISO certifications play a crucial role in the pharmaceutical industry by ensuring quality, efficiency, safety, and compliance with...
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Jyotsna Sharma
Jul 17, 202313 min read
Upholding the Walter® Standard: Cultivating Excellence Through Quality Control in Pharma Industry
Commitment towards excellence and putting quality first for the well-being of every consumer is a responsibility of every pharmaceutical...
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PharmaWalt
May 4, 20233 min read
Maintaining Aseptic Conditions: The Key to Producing Safe and Effective Sterile Medicines
Maintaining aseptic conditions in pharmaceutical sterile areas is crucial to prevent contamination and ensure the production of safe and...
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