Tag: Pharmaceutical manufacturing under GMP

How ANVISA GMP Helps Prevent Pharmaceutical Contamination in Brazil

December 25, 2024 digi

How ANVISA GMP Helps Prevent Pharmaceutical Contamination in Brazil How ANVISA GMP Helps Prevent Pharmaceutical Contamination in Brazil Introduction to ANVISA GMP and Pharmaceutical Contamination The National Health Surveillance Agency (ANVISA) is Brazil’s regulatory authority responsible for overseeing the safety, efficacy, and quality of pharmaceutical products. One of the primary ways ANVISA ensures drug safety…

GMP in Latin America (ANVISA, COFEPRIS)

How TGA GMP Affects Pharmaceutical Manufacturing Risk Management

December 25, 2024 digi

How TGA GMP Affects Pharmaceutical Manufacturing Risk Management The Role of TGA GMP in Pharmaceutical Risk Management Introduction to TGA GMP and Risk Management Pharmaceutical manufacturing is inherently complex, involving numerous processes, raw materials, and regulatory requirements. Ensuring product safety, efficacy, and quality requires effective risk management strategies. The Therapeutic Goods Administration (TGA) enforces stringent…

TGA GMP Guidelines

Schedule M (Revised) GMP for the Manufacture of Biologics and Biosimilars

December 25, 2024 digi

Schedule M (Revised) GMP for the Manufacture of Biologics and Biosimilars Ensuring Quality and Compliance in the Manufacture of Biologics and Biosimilars Under Schedule M (Revised) GMP Introduction to Biologics, Biosimilars, and Schedule M (Revised) Biologics and biosimilars are among the most advanced pharmaceutical products, offering targeted treatments for diseases such as cancer, autoimmune disorders,…

SCHEDULE - M - Revised

The Challenges of PMDA GMP Compliance in the Pharmaceutical Industry

December 25, 2024 digi

The Challenges of PMDA GMP Compliance in the Pharmaceutical Industry The Challenges of PMDA GMP Compliance in the Pharmaceutical Industry Introduction to PMDA GMP Compliance Good Manufacturing Practices (GMP) are essential to ensuring that pharmaceutical products are consistently produced and controlled according to quality standards. In Japan, the Pharmaceutical and Medical Devices Agency (PMDA) is…

PMDA GMP Guidelines

How NMPA GMP Helps Manage Risk in Pharmaceutical Manufacturing

December 25, 2024 digi

How NMPA GMP Helps Manage Risk in Pharmaceutical Manufacturing How NMPA GMP Helps Manage Risk in Pharmaceutical Manufacturing Introduction to NMPA GMP and Risk Management The pharmaceutical industry is one of the most heavily regulated sectors globally due to the potential risks associated with drug manufacturing, distribution, and usage. Ensuring the safety, efficacy, and quality…

NMPA GMP Guidelines

Best Practices for Ensuring EMA GMP Compliance in Pharmaceutical R&D

December 24, 2024 digi

Best Practices for Ensuring EMA GMP Compliance in Pharmaceutical R&D Ensuring EMA GMP Compliance in Pharmaceutical Research and Development Introduction to EMA GMP in Pharmaceutical R&D Pharmaceutical research and development (R&D) is the foundation of creating innovative drugs that improve patient outcomes. While R&D primarily focuses on discovery and preclinical studies, compliance with the European…

EMA GMP Guidelines

How to Use WHO GMP Guidelines to Improve Manufacturing Efficiency

December 24, 2024 digi

How to Use WHO GMP Guidelines to Improve Manufacturing Efficiency Enhancing Manufacturing Efficiency with WHO GMP Guidelines Introduction to Manufacturing Efficiency and WHO GMP Manufacturing efficiency is a cornerstone of the pharmaceutical industry, ensuring the consistent production of high-quality medicines while optimizing resources and minimizing costs. The World Health Organization (WHO)’s Good Manufacturing Practices (GMP))…

WHO GMP Guidelines

MHRA GMP Guidelines for Clinical Manufacturing: What Pharma Companies Need to Know

December 24, 2024 digi

MHRA GMP Guidelines for Clinical Manufacturing: What Pharma Companies Need to Know Understanding MHRA GMP Guidelines for Clinical Manufacturing Introduction to Clinical Manufacturing and MHRA GMP Clinical manufacturing refers to the production of investigational medicinal products (IMPs) used in clinical trials. These products are critical for evaluating the safety, efficacy, and quality of new drugs…

MHRA GMP Guidelines

The Role of TGA GMP in Quality Assurance and Control

December 24, 2024 digi

The Role of TGA GMP in Quality Assurance and Control How TGA GMP Ensures Excellence in Quality Assurance and Control Introduction to TGA GMP and Quality Assurance The Therapeutic Goods Administration (TGA) enforces stringent Good Manufacturing Practices (GMP) to regulate the production and distribution of pharmaceutical products in Australia. A cornerstone of TGA GMP compliance…

TGA GMP Guidelines

The Role of Documentation in Achieving ANVISA GMP Compliance

December 24, 2024 digi

The Role of Documentation in Achieving ANVISA GMP Compliance The Role of Documentation in Achieving ANVISA GMP Compliance Introduction to ANVISA GMP and the Importance of Documentation The National Health Surveillance Agency (ANVISA) plays a critical role in ensuring the safety, quality, and efficacy of pharmaceutical products in Brazil. One of the primary regulatory frameworks…

GMP in Latin America (ANVISA, COFEPRIS)