Tag: Pharmaceutical supply chain GMP

How to Ensure Compliance with FDA and Health Canada’s GMP for OTC Drugs

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How to Ensure Compliance with FDA and Health Canada’s GMP for OTC Drugs Practical Tips for Ensuring GMP Compliance for OTC Drugs under FDA and Health Canada Introduction to GMP Compliance for OTC Drugs Over-the-counter (OTC) drugs are widely available to consumers without a prescription, making their safety, quality, and efficacy critical for public health….

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GMP in North America (FDA, Health Canada)

How PMDA’s GMP Guidelines Support Pharmaceutical Product Development in Japan

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How PMDA’s GMP Guidelines Support Pharmaceutical Product Development in Japan A Step-by-Step Guide to PMDA’s GMP Guidelines for Pharmaceutical Product Development in Japan Introduction to PMDA and GMP Guidelines The Pharmaceuticals and Medical Devices Agency (PMDA) in Japan plays a critical role in ensuring the safety, efficacy, and quality of pharmaceutical products. Its Good Manufacturing…

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GMP in Asia (PMDA, NMPA, KFDA)

Best Practices for GMP Documentation in North America

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Best Practices for GMP Documentation in North America Comprehensive Best Practices for GMP Documentation in North America Introduction to GMP Documentation Documentation is a critical component of Good Manufacturing Practices (GMP), ensuring consistency, traceability, and compliance with regulatory requirements. In North America, both the Food and Drug Administration (FDA) and Health Canada emphasize the importance…

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GMP in North America (FDA, Health Canada)

The Role of GMP in Regulatory Approval for Drugs in Asia

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The Role of GMP in Regulatory Approval for Drugs in Asia How GMP Compliance Supports Regulatory Approval for Drugs in Asia Introduction to GMP and Regulatory Approvals Good Manufacturing Practices (GMP) are the foundation of pharmaceutical quality, ensuring that drugs are consistently produced and controlled according to established standards. Regulatory authorities in Asia, such as…

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GMP in Asia (PMDA, NMPA, KFDA)

How to Ensure GMP Compliance for Pharma Manufacturing in Both the US and Canada

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How to Ensure GMP Compliance for Pharma Manufacturing in Both the US and Canada Expert Guide to Achieving GMP Compliance for Pharmaceutical Manufacturing in the US and Canada Introduction to GMP Compliance in North America The pharmaceutical industry in North America is governed by stringent regulatory requirements to ensure the safety, efficacy, and quality of…

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GMP in North America (FDA, Health Canada)

How to Build a GMP-Compliant Pharmaceutical Facility in Asia

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How to Build a GMP-Compliant Pharmaceutical Facility in Asia Step-by-Step Guide to Building a GMP-Compliant Pharmaceutical Facility in Asia Introduction to GMP-Compliant Facilities A Good Manufacturing Practices (GMP)-compliant pharmaceutical facility is critical for ensuring the production of high-quality, safe, and effective medicines. Regulatory authorities in Asia, such as Japan’s Pharmaceuticals and Medical Devices Agency (PMDA),…

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GMP in Asia (PMDA, NMPA, KFDA)

FDA and Health Canada’s GMP Requirements for Drug Imports and Exports

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FDA and Health Canada’s GMP Requirements for Drug Imports and Exports A Complete Guide to FDA and Health Canada GMP Requirements for Drug Imports and Exports Introduction to GMP Compliance for Drug Imports and Exports The pharmaceutical industry operates in a global marketplace where drugs are frequently imported and exported across borders. Ensuring compliance with…

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GMP in North America (FDA, Health Canada)

The Relationship Between GMP and Regulatory Authorities in Asia

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The Relationship Between GMP and Regulatory Authorities in Asia Understanding the Connection Between GMP and Regulatory Authorities in Asia Introduction to GMP and Regulatory Authorities Good Manufacturing Practices (GMP) are essential for ensuring the quality, safety, and efficacy of pharmaceutical products. Regulatory authorities in Asia, such as Japan’s Pharmaceuticals and Medical Devices Agency (PMDA), China’s…

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GMP in Asia (PMDA, NMPA, KFDA)

How to Prepare Your Pharmaceutical Facility for FDA GMP Inspections

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How to Prepare Your Pharmaceutical Facility for FDA GMP Inspections Comprehensive Guide to Preparing Your Pharmaceutical Facility for FDA GMP Inspections Introduction to FDA GMP Inspections The Food and Drug Administration (FDA) conducts Good Manufacturing Practices (GMP) inspections to ensure that pharmaceutical facilities meet the highest standards of safety, quality, and compliance. These inspections are…

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GMP in North America (FDA, Health Canada)

How to Achieve GMP Compliance for Pharma Exporters to Asia

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How to Achieve GMP Compliance for Pharma Exporters to Asia Step-by-Step Guide to Achieving GMP Compliance for Pharmaceutical Exporters to Asia Introduction to GMP Compliance in Asia Good Manufacturing Practices (GMP) are critical for ensuring the safety, efficacy, and quality of pharmaceutical products. Regulatory authorities across Asia, such as Japan’s Pharmaceuticals and Medical Devices Agency…

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GMP in Asia (PMDA, NMPA, KFDA)