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Amoxycillin-Clavulanic Acid Formulation: A Powerful Dual-Action Antibiotic Formula
It provides essential coverage for a wide range of conditions, from respiratory and skin infections to various mixed bacterial ailments across all age groups, particularly when single-agent antibiotics fail.
The power of this formulation lies in its strategic, dual-action mechanism. Amoxycillin offers potent, broad-spectrum bactericidal activity. Simultaneously, Clavulanic Acid acts as a guardian, breaking down the resistance mechanisms that bacteria use to neutralize the a
Akshay Gautam
2 days ago11 min read


Understanding Evaporation in Pharmaceuticals
In the fast-evolving world of pharmaceutical manufacturing, the operation of evaporation is far more than simple solvent removal. It is a mission-critical, scientifically engineered transformation that directly determines product quality, therapeutic potency, and regulatory success. Achieving precise concentration through controlled evaporation is a cornerstone of product stability, bioavailability, shelf life, and successful downstream processing.
Akshay Gautam
Nov 1511 min read


Beyond the Bubble: Effervescent Tablets in Pharmaceuticals
The blog is the quick idea for the basic idea about effervescent, what they are, how they work, basic insight for composition, and easy effective execution.
Akshay Gautam
Nov 810 min read


Dryers in Pharmaceutical Manufacturing: Ensuring Efficiency, Quality, and Product Stability
The blog is a quick insight into the process of the pharmaceutical drying. highlighting its importance alongside the types of the frequently used dryers, making the process effective and engaging with the development of a stable, quality product.
Akshay Gautam
Nov 112 min read


WHO GMP vs Indian GMP: A Manufacturer’s Guide to GMP
the blog provide idea about Good Manufacturing Practices (GMP) are the foundation of quality in the pharmaceutical industry. They ensure that every medicine is consistently safe, effective, and of high quality. This commitment to excellence protects public health and builds trust in medicines worldwide.
Globally, the World Health Organization (WHO) provides comprehensive GMP guidelines. The most important ones are TRS 986 Annex 2 for general GMP and TRS 1044 Annex 2 for ster
Akshay Gautam
Oct 1813 min read


Healing Without Harming: Sustainable Pharma for a Greener Tomorrow
the blog provides idea about the pharmaceutica industry, while saving lives, also leaves a heavy ecological footprint through high water usage, energy demands, plastic packaging, chemical waste, and global supply chains. This blog explores how sustainability is transforming pharma, from green chemistry and renewable energy to eco-friendly packaging innovations like glass jars, aluminum caps, and paper-based blisters. It reviews regulatory frameworks in India and globally, whi
Akshay Gautam
Sep 67 min read


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 308 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 166 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 810 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
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