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  • "Its a long established fact that a reader will be distracted by the readable content of a page when"We are pleased to inform that one highly experienced."
  • For any requirement regarding on-site, write to us at
  • KNORSPHARMA@GMAIL.COM OR CALL AT 9878880408
Facebook Twitter Linkedin Instagram
Knors Pharma
  • Home
  • Team of Experts
    • Dr. Rajesh Kaushik
    • Ms. Priyanka Dhawan
    • Er. R. S. Bansal
    • Ms. Kusum Seth
    • Mr. S.P. Singh
    • Ms. Balwinder Kaur
    • Mr. Arun Prasad
    • Mr. Saaraj Gupta
    • Mr. Amit
    • Mr. Sushant Sagar Pokhriyal
  • Gallery
  • Services We Offer
    • Audits
    • Consultancy
    • Training
    • Regulatory Affairs
    • Suppliers Qualifications
    • Pharma Auditors
    • GAP Analysis
    • Due Diligence
  • News & Blogs
    • Industry Outlook
    • Latest Blogs
  • Contact Us
  • "Its a long established fact that a reader will be distracted by the readable content of a page when"We are pleased to inform that one highly experienced."
  • For any requirement regarding on-site, write to us at
  • KNORSPHARMA@GMAIL.COM OR CALL AT 9878880408
Facebook Twitter Linkedin Instagram
Knors Pharma
  • Home
  • Team of Experts
    • Dr. Rajesh Kaushik
    • Ms. Priyanka Dhawan
    • Er. R. S. Bansal
    • Ms. Kusum Seth
    • Mr. S.P. Singh
    • Ms. Balwinder Kaur
    • Mr. Arun Prasad
    • Mr. Saaraj Gupta
    • Mr. Amit
    • Mr. Sushant Sagar Pokhriyal
  • Gallery
  • Services We Offer
    • Audits
    • Consultancy
    • Training
    • Regulatory Affairs
    • Suppliers Qualifications
    • Pharma Auditors
    • GAP Analysis
    • Due Diligence
  • News & Blogs
    • Industry Outlook
    • Latest Blogs
  • Contact Us
Read more about the article How Do Revised Schedule M Guidelines Challenge the Pharmaceutical Organizations?

How Do Revised Schedule M Guidelines Challenge the Pharmaceutical Organizations?

  • Post author:knorspharma_admin
  • Post published:September 26, 2025
  • Post category:Blog

The Indian pharma scene is changing super fast. Following the rules is way more important than anything else. The provisions of the revised Schedule M have introduced basic standards for…

Continue ReadingHow Do Revised Schedule M Guidelines Challenge the Pharmaceutical Organizations?
Read more about the article How to Choose the Right Pharma GMP Auditors for Your Manufacturing Unit?

How to Choose the Right Pharma GMP Auditors for Your Manufacturing Unit?

  • Post author:knorspharma_admin
  • Post published:September 12, 2025
  • Post category:Blog

Pharma GMP auditors play a crucial role in ensuring product quality and maintaining regulatory compliance. Strict compliance with Good Manufacturing Practices (GMP) is mandatory for every pharmaceutical manufacturing unit. In…

Continue ReadingHow to Choose the Right Pharma GMP Auditors for Your Manufacturing Unit?
Read more about the article Learning from Recent Regulatory Inspections

Learning from Recent Regulatory Inspections

  • Post author:knorspharma_admin
  • Post published:August 21, 2025
  • Post category:Blog

Regulatory inspections in the pharmaceutical industry have the huge purpose of regulatory inspection that always ensures the safety, efficacy, and quality of medications. This is useful to ensure compliance with…

Continue ReadingLearning from Recent Regulatory Inspections
Read more about the article How Can AI Help in the Better Implementation of GxPs?

How Can AI Help in the Better Implementation of GxPs?

  • Post author:knorspharma_admin
  • Post published:July 18, 2025
  • Post category:Blog

GxPs are "Good Practices" of pharma that include GMP, GCP, GDP, GLP, etc. And they are a must-have for regulations, quality, and safety. The applications of AI in GxPs are…

Continue ReadingHow Can AI Help in the Better Implementation of GxPs?
Read more about the article Understanding Pharma Regulatory Consultants: What They Do and Why It Matters

Understanding Pharma Regulatory Consultants: What They Do and Why It Matters

  • Post author:knorspharma_admin
  • Post published:July 3, 2025
  • Post category:Blog

At present, in 2025, the pharmaceutical industry is one of the most regulated markets. To succeed in this business, it is important that compliance with all the necessities is observed.…

Continue ReadingUnderstanding Pharma Regulatory Consultants: What They Do and Why It Matters
Read more about the article What is GMP Compliance in the Pharmaceutical Industry: An Ultimate Guide

What is GMP Compliance in the Pharmaceutical Industry: An Ultimate Guide

  • Post author:knorspharma_admin
  • Post published:June 24, 2025
  • Post category:Blog

Each product in the pharmaceutical industry must meet safety, quality, and efficacy standards according to Good Manufacturing Practices (GMP). GMP compliance helps maintain the tough regulations that come from different…

Continue ReadingWhat is GMP Compliance in the Pharmaceutical Industry: An Ultimate Guide
Read more about the article Importance of GAP Analysis in Pharma Industry

Importance of GAP Analysis in Pharma Industry

  • Post author:knorspharma_admin
  • Post published:June 5, 2025
  • Post category:Blog

The pharmaceutical industry is one of the most heavily controlled and detailed in the world. The pharmaceutical companies have to keep up with rules, maintain high quality, and improve their…

Continue ReadingImportance of GAP Analysis in Pharma Industry
Read more about the article Importance of Due Diligence in the Pharmaceutical Industry

Importance of Due Diligence in the Pharmaceutical Industry

  • Post author:knorspharma_admin
  • Post published:May 28, 2025
  • Post category:Blog

In the pharmaceutical sector, technical due diligence (TDD) is absolutely vital. It guarantees that every element of a company's operations, regulatory compliance, and financial situation is carefully evaluated. Protecting corporate…

Continue ReadingImportance of Due Diligence in the Pharmaceutical Industry
Read more about the article Keeping Quality Oversight in Pharmaceutical Operations

Keeping Quality Oversight in Pharmaceutical Operations

  • Post author:knorspharma_admin
  • Post published:May 12, 2025
  • Post category:Blog

Quality oversight in pharmaceuticals industry refers to systematically supervising processes, materials, and products to ensure they meet regulatory, safety, and efficacy standards throughout the drug development lifecycle. Quality oversight is…

Continue ReadingKeeping Quality Oversight in Pharmaceutical Operations
Read more about the article Importance of Robust Product Development or QbD in Pharma Industry: Overview of Quality by Design

Importance of Robust Product Development or QbD in Pharma Industry: Overview of Quality by Design

  • Post author:knorspharma_admin
  • Post published:April 25, 2025
  • Post category:Blog

The demand and importance of robust product development, particularly through the approach of overview of quality by design, cannot be overstated in the pharmaceutical industry. QbD (Quality by Design in…

Continue ReadingImportance of Robust Product Development or QbD in Pharma Industry: Overview of Quality by Design
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