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8 Articles

Cleanrooms × Commissioning × Computerised System Validation × Sanitization Procedures × Quality ×

Change Management

Change Management

* Introduction * Change is inevitable in the pharmaceutical industry, where advancements in technology, regulatory updates, and operational improvements constantly reshape the landscape. However, impl...

Quality

Jan 31, 2025

Self-inspection, quality audits

Self-inspection, quality audits

** Introduction: ** What is an Audit? According to ISO 19011, an audit is a systematic, independent, and documented process for obtaining objective evidence and evaluating it objectively to determine ...

Quality

Mar 27, 2024

Quality Management QMS

Quality Management QMS

** Introduction: ** At the heart of GMP lies the commitment to ensuring that medicinal and food products meet the quality standards necessary for their intended use. As stated in GMP guidelines, Qual...

Quality

Mar 26, 2024

Computerised Systems

Computerised Systems

** Introduction: ** In the dynamic world of pharmaceuticals, the integration of computerized systems is not just a technological advancement; it's a critical component ensuring patient safety, product...

Computerised System Validation Validation

Dec 6, 2023

Cleanrooms in Pharmaceuticals Facilities

Cleanrooms in Pharmaceuticals Facilities

** Introduction: ** Cleanrooms play a pivotal role in pharmaceutical facilities, contributing to product safety, quality, and efficacy. These specialized environments are meticulously designed and mai...

Cleanrooms Facility

Oct 26, 2023

Sanitization Procedures

Sanitization Procedures

** Introduction: ** In the world of pharmaceutical and food manufacturing, ensuring the highest level of product safety is paramount. The Good Manufacturing Practices (GMP) standards, established by t...

Facility Sanitization Procedures

Oct 19, 2023

Commissioning, Qualification, and Validation

Commissioning, Qualification, and Validation

Start writing here... *Introduction* In the realm of pharmaceutical manufacturing, quality and safety are of paramount importance. Adhering to Good Manufacturing Practices (GMP) is not merely a ...

Commissioning Facility Qualification Validation

Oct 12, 2023

Annual Product Review in Pharma

Safaa Abdel Wahab

Annual Product Review in Pharma

*Introduction:* In the pharmaceutical industry, adhering to Good Manufacturing Practices (GMP) regulations is paramount. These regulations necessitate the generation and analysis of a substantial volu...

Annual Product Review Quality

Oct 8, 2023

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Annual Product Review