Tag: PMDA GMP (Japan)

How Schedule M (Revised) GMP Helps with Drug Stability and Shelf Life

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How Schedule M (Revised) GMP Helps with Drug Stability and Shelf Life Ensuring Drug Stability and Shelf Life Through Schedule M (Revised) GMP Guidelines Introduction to Drug Stability and Shelf Life Drug stability and shelf life are critical parameters in pharmaceutical manufacturing. They ensure that a drug maintains its intended efficacy, safety, and quality throughout…

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SCHEDULE - M - Revised

The Role of WHO GMP in Regulatory Approvals for Emerging Markets

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The Role of WHO GMP in Regulatory Approvals for Emerging Markets How WHO GMP Guidelines Facilitate Regulatory Approvals in Emerging Markets Introduction to WHO GMP and Emerging Markets Emerging markets are rapidly becoming vital players in the global pharmaceutical industry, driven by growing healthcare demands and expanding manufacturing capabilities. However, gaining regulatory approval in these…

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WHO GMP Guidelines

How to Ensure GMP Compliance with MHRA Guidelines for Biologics

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How to Ensure GMP Compliance with MHRA Guidelines for Biologics Ensuring GMP Compliance with MHRA Guidelines for Biologics Introduction to MHRA GMP Guidelines for Biologics Biologics, or biopharmaceuticals, are complex medicinal products derived from living organisms. These include vaccines, monoclonal antibodies, gene therapies, and cell-based products. Due to their intricate nature and sensitivity to environmental…

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MHRA GMP Guidelines

The Role of Technology in Achieving NMPA GMP Compliance

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The Role of Technology in Achieving NMPA GMP Compliance The Role of Technology in Achieving NMPA GMP Compliance Introduction to NMPA GMP and Technology The pharmaceutical industry is one of the most highly regulated sectors globally, with strict standards in place to ensure the safety, efficacy, and quality of drugs. In China, the National Medical…

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NMPA GMP Guidelines

How to Achieve GMP Compliance in TGA Regulated Clinical Trials

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How to Achieve GMP Compliance in TGA Regulated Clinical Trials Ensuring GMP Compliance in TGA-Regulated Clinical Trials Introduction to GMP Compliance in Clinical Trials Clinical trials are critical for evaluating the safety and efficacy of new pharmaceutical products. The Therapeutic Goods Administration (TGA) in Australia enforces stringent Good Manufacturing Practices (GMP) to ensure the quality,…

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TGA GMP Guidelines

PMDA GMP Guidelines for the Manufacture of Injectable Drugs

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PMDA GMP Guidelines for the Manufacture of Injectable Drugs PMDA GMP Guidelines for the Manufacture of Injectable Drugs Introduction to PMDA GMP and Injectable Drugs Injectable drugs are among the most critical pharmaceutical products, as they are administered directly into the body, often for serious medical conditions. The safety and efficacy of injectable drugs depend…

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PMDA GMP Guidelines

How COFEPRIS GMP Guidelines Address the Issue of Counterfeit Drugs in Mexico

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How COFEPRIS GMP Guidelines Address the Issue of Counterfeit Drugs in Mexico How COFEPRIS GMP Guidelines Address the Issue of Counterfeit Drugs in Mexico Introduction to COFEPRIS and the Counterfeit Drug Problem The Federal Commission for the Protection against Sanitary Risks (COFEPRIS) is the regulatory body responsible for ensuring the safety, quality, and efficacy of…

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GMP in Latin America (ANVISA, COFEPRIS)

How EMA GMP Standards Promote Sustainability in Pharmaceutical Manufacturing

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How EMA GMP Standards Promote Sustainability in Pharmaceutical Manufacturing Sustainability in Pharmaceutical Manufacturing with EMA GMP Standards Introduction to Sustainability and EMA GMP Standards Sustainability has become a critical consideration in pharmaceutical manufacturing as the industry seeks to reduce its environmental footprint while maintaining high standards of quality and safety. The European Medicines Agency (EMA)’s…

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EMA GMP Guidelines

How WHO GMP Guidelines Influence Drug Packaging and Labeling

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How WHO GMP Guidelines Influence Drug Packaging and Labeling Understanding the Impact of WHO GMP Guidelines on Drug Packaging and Labeling Introduction to Drug Packaging and Labeling under WHO GMP Drug packaging and labeling are critical components of pharmaceutical manufacturing, playing a vital role in ensuring product integrity, patient safety, and regulatory compliance. The World…

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WHO GMP Guidelines

Common Schedule M (Revised) GMP Violations and How to Avoid Them

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Common Schedule M (Revised) GMP Violations and How to Avoid Them Identifying and Avoiding Common Schedule M (Revised) GMP Violations Introduction to Schedule M (Revised) GMP Compliance Schedule M (Revised), under the Drugs and Cosmetics Act, 1940, sets forth stringent Good Manufacturing Practices (GMP) to ensure the safety, efficacy, and quality of pharmaceutical products. Compliance…

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SCHEDULE - M - Revised