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The MHRA Orange Guide provides comprehensive regulations and essential guidance for pharmaceutical manufacturers and distributors operating in the UK. This critical resource covers Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and other vital aspects of regulatory compliance, ensuring high standards for medicine production and supply within the UK.

Explore the intricate landscape of China's drug practices and policies, delving into the nation's regulatory frameworks, manufacturing standards, and public health initiatives. This content examines how Chinese authorities manage pharmaceutical production, distribution, and consumption, highlighting the unique challenges and strategies employed in shaping the country's drug control and healthcare systems.

Explore the critical legal and tax framework governing India's dynamic Pharmaceutical and Life Science industries. Understand the regulatory environment, compliance requirements, and taxation policies that shape business operations and investment in this rapidly growing sector. This overview is essential for stakeholders navigating the complexities of Indian healthcare and biotech.

Explore the definitive FDA Deskbook, your essential compliance and enforcement guide for navigating complex regulatory landscapes. This comprehensive resource offers in-depth insights into Food and Drug Administration standards, aiding professionals in ensuring adherence and mitigating risks associated with regulatory enforcement.

Explore the official "Japanese Pharmacopoeia," a critical reference detailing drug standards and pharmaceutical regulations for quality control in Japan. This essential publication outlines specifications for drug ingredients, preparations, and testing methods, ensuring public health and safety across the nation's pharmaceutical industry.

Navigating EU regulatory procedures is crucial for market access within the European Union, encompassing strict guidelines for various industries. Professionals often rely on resources like The Organisation for Professionals in Regulatory Affairs (TOPRA) to stay informed and ensure compliance with the complex European regulatory framework.

Explore the comprehensive landscape of Active Pharmaceutical Ingredients (APIs), from their initial development and complex manufacturing processes to the critical regulatory frameworks ensuring drug safety and efficacy. This encompasses the entire journey of drugs within the pharmaceutical sciences, highlighting innovation, production, and compliance.