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Person measuring a sample on an analytical balance

Analytical Balances for QC Labs Purposes: Proper Weighing Practices

Explore the critical role of analytical balances in QC labs, focusing on operational principles, performance factors, and compliance with industry...
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Quality Risk Management Process

Quality Risk Management in the Pharmaceutical Industry

Explore the essentials of Quality Risk Management in Pharma: Principles, tools, guidelines, and implementation strategies for enhanced safety....
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A hand pointing on a screen with chromatograms showing peak tailing

Peak Tailing in Chromatography: Troubleshooting Basics

Explore the essentials of troubleshooting peak tailing, including pro tips, and suggestions for accurate and reliable chromatography....
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Defining Specification Limits for Unknown, Known and Total Impurities in New Drug Products with HPLC

Defining Specification Limits for Impurities in New Drug Products

Learn how pharmaceutical manufacturers define specification limits for known, unknown, and total impurities in new drug products, ensuring safety and...
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User Requirement Specification for Purchase of Manufacturing Equipment

User Requirement Specification: How to Create URS for Successful Equipment Procurement

Explore the essentials of User Requirement Specification (URS) for successful project execution. Learn to craft effective URS documents....
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Person working in QC Lab - LC

Impurities in Pharmaceuticals: Types, Regulations and Strategies

Discover the essential information about impurities in pharmaceuticals, their types, and how they impact drug quality. Learn about regulatory requirements,...
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Good Documentation Practice - FI

Good Documentation Practice: Ensuring Data Integrity and Compliance in the Pharmaceutical Industry

Explore effective strategies for maintaining clear and comprehensive records with our guide on good documentation practices, ensuring accuracy and reliability....
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GMP Cleanroom

GMP Cleanroom Classifications: Understand Class A, B, C and D

Learn GMP cleanroom classes A, B, C, D for contamination control in pharmaceuticals. Understand air cleanliness & particle counts for...
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Electronic Quality Management System eQMS

Electronic Quality Management Systems – eQMS

Optimize compliance and quality control in the pharmaceutical industry with eQMS (Electronic Quality Management System). Streamline documentation, enhance regulatory adherence,...
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GMP Regulatory Bodies

GMP Regulatory Bodies: Understanding the Key Differences

Explore global GMP standards with regulatory bodies like FDA, EMA, and WHO. Ensure compliance for pharmaceutical quality and safety worldwide....
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