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Good Documentation Practices in Pharma: ALCOA+ Explained with Examples

22/01/2026 by admin
Good Documentation Practices in Pharma

In the pharmaceutical industry, documentation is more than a regulatory formality—it is legal evidence that products are consistently manufactured and …

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Change Control in Pharmaceuticals: Step-by-Step Implementation Guide

20/01/2026 by admin

In the highly regulated pharmaceutical industry, even the smallest modification can have a significant impact on product quality, patient safety, …

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Deviation Management in Pharma: Root Cause Analysis and CAPA System

18/01/2026 by admin

In the highly regulated pharmaceutical industry, maintaining product quality, patient safety, and regulatory compliance is non-negotiable. Even minor deviations from …

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Data Integrity in Pharma: A Guide to ALCOA+

04/01/2026 by admin
Data Integrity in Pharma

In today’s highly regulated pharmaceutical industry, data integrity in pharma has become a critical pillar for ensuring product quality, patient …

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The Ultimate Guide to GMP in Pharmaceuticals: 9 Critical Compliance Principles

21/12/2025 by admin

Quality, safety, and efficacy are the foundations of every pharmaceutical product that reaches a patient. Medicines are not ordinary consumer …

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Technology Transfer in Pharmaceuticals: Process, Challenges, and Best Practices

14/12/2025 by admin
Technology Transfer in Pharma

The pharmaceutical industry operates in a highly regulated environment where product quality, safety, and efficacy must remain consistent throughout a …

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Equipment Qualification in Pharma: DQ, IQ, OQ, PQ Complete Guide for Professionals

07/12/2025 by admin
Equipment Qualification in Pharma

In the pharmaceutical industry, equipment plays a critical role in ensuring the manufacturing of safe, effective, and high-quality products. Regulatory …

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Cross-Contamination Control in Pharmaceutical Manufacturing: Prevention and Compliance

30/11/2025 by admin
Cross-Contamination Control in Pharma

In the pharmaceutical industry, maintaining product purity is not just a regulatory requirement—it is a moral obligation that directly impacts …

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In-Process Controls in Pharmaceutical Manufacturing: Importance and Examples

23/11/2025 by admin

Quality is the backbone of the pharmaceutical industry. Every tablet, capsule, vial, or ointment must meet strict standards of identity, …

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Hold Time Study in Pharma Explained: A Complete GMP Guide

18/11/2025 by admin
Hold Time Study

The pharmaceutical industry is driven by strict quality control requirements, regulatory guidelines, and Good Manufacturing Practices (GMP). Among all the …

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  • Good Documentation Practices in PharmaGood Documentation Practices in Pharma: ALCOA+ Explained with Examples
    In Validation & Qualification
    22/01/2026
  • Change Control in Pharmaceuticals: Step-by-Step Implementation Guide
    In Pharma Engineering
    20/01/2026
  • Deviation Management in Pharma: Root Cause Analysis and CAPA System
    In Validation & Qualification
    18/01/2026
  • Data Integrity in PharmaData Integrity in Pharma: A Guide to ALCOA+
    In Pharma Engineering
    04/01/2026
  • The Ultimate Guide to GMP in Pharmaceuticals: 9 Critical Compliance Principles
    In Validation & Qualification
    21/12/2025

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