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Explore the critical role of green chemistry in transforming the pharmaceutical industry towards more sustainable practices. This approach emphasizes eco-friendly drug manufacturing, minimizing waste, and reducing the environmental footprint of drug production. Discover how pharmaceutical green practices are not only enhancing operational efficiency but also contributing to safer and more environmentally responsible pharmaceutical development, paving the way for truly sustainable pharmaceuticals.

Bhaisajya Kalpana Vijnana is the foundational Ayurvedic pharmaceutical science dedicated to the intricate art and science of herbal medicine formulation. This discipline encompasses the detailed study and practical application of various processes involved in transforming raw medicinal materials into effective Ayurvedic drug preparations, ensuring their potency, stability, and therapeutic efficacy. It's crucial for anyone studying or practicing Ayurvedic pharmacology and understanding the rich heritage of traditional Indian medicine.

Dive into Uncle Fester's controversial guide exploring alleged methods for methamphetamine synthesis. This resource often appears in discussions around clandestine chemistry and illicit drug manufacturing, offering insights into the alleged processes involved in creating this substance.

Explore the dynamic landscape of the Indian pharmaceutical industry, a global leader in generic drug manufacturing. This sector is a cornerstone of India's economy, renowned for its extensive pharmaceutical exports and housing many of the top pharma companies, significantly contributing to worldwide healthcare accessibility.

Dive deep into the engineering principles of pharmaceutical production with this comprehensive guide. Learn about drug manufacturing processes, quality control, and essential GMP standards for efficient and compliant biopharmaceutical manufacturing.

Dive into the comprehensive world of pharmaceutical technology with this essential encyclopedia. It covers cutting-edge advancements in drug development, innovative manufacturing processes, and the foundational pharmaceutical science. An invaluable resource for researchers, students, and professionals seeking in-depth knowledge on the methods and tools shaping modern medicine.

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 core principles and practical applications of pharmaceutical engineering, covering everything from drug development to scalable manufacturing processes. This includes facility design, regulatory compliance (like GMP), process optimization, and ensuring the quality and safety of medicines across various biopharmaceutical and chemical drug production cycles.

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.

This comprehensive handbook, Volume Three, provides essential insights and detailed formulations specifically for pharmaceutical liquid products. It serves as an invaluable resource for professionals seeking best practices, manufacturing processes, and quality standards for developing various liquid dosage forms in the pharmaceutical industry.

These comprehensive lecture notes offer an in-depth exploration of pharmaceutical microbiology, covering essential topics such as microbial contamination control, aseptic processing, sterility testing, and regulatory requirements crucial for drug manufacturing. Ideal for students and professionals seeking to understand the critical role of microbiology in the pharmaceutical industry.

Ensuring microbial contamination control is paramount in the highly regulated field of parenteral drug manufacturing. This critical aspect of pharmaceutical sciences involves stringent aseptic processing and robust quality control measures to guarantee patient safety and product integrity. Understanding and implementing effective strategies for contamination management is essential for all pharmaceutical professionals.

This comprehensive guide delves into Good Manufacturing Practices (GMP) for pharmaceuticals, outlining a meticulous plan for total quality control. From initial manufacturing stages to the final consumer, this fifth edition is a vital resource in the pharmaceutical sciences, ensuring robust standards across the drug production lifecycle.

Explore the foundational principles of pharmaceutical microbiology with this essential 1st Edition guide. Delve into crucial topics like microbial quality control, ensuring product sterility, and understanding contamination risks within drug manufacturing. This resource is indispensable for professionals and students seeking comprehensive insights into the unique microbiological challenges and regulatory requirements of the pharmaceutical industry.

Explore the fundamental unit processes critical to pharmacy and pharmaceutical engineering. This encompasses various operations essential for drug manufacturing, formulation, and ensuring the quality and efficacy of medicinal products.