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This comprehensive series explores the vital processes of drug safety evaluation, crucial at every stage of pharmaceutical development. It covers essential methodologies for assessing medication safety, understanding pharmacovigilance principles, and ensuring robust safety profiles for new drugs, serving as an invaluable resource for industry professionals and researchers.

This comprehensive handbook serves as an essential guide for professionals involved in pharmaceutical development, meticulously detailing the critical aspects of stability testing. It thoroughly explores current regulations, established methodologies, and industry best practices to ensure product quality and compliance throughout the drug lifecycle, providing invaluable insights for researchers and quality assurance teams.

The year 1979 proved to be a pivotal period for nuclear medicine, showcasing significant advancements in diagnostic imaging and the development of radiopharmaceuticals. These innovations greatly enhanced the field's capacity for non-invasive disease detection, ultimately improving patient care. This era solidified nuclear medicine's crucial role in medical diagnostics and research, laying groundwork for future breakthroughs.

Delve into the comprehensive world of biopharmaceutics, exploring its foundational principles and critical applications across various therapeutic areas. This essential resource also provides insights into the latest developments and emerging trends that are shaping the future of drug discovery and patient care in the biopharmaceutical sector.

Explore the crucial concepts and practical applications central to pediatric drug development. This resource comprehensively addresses the unique considerations for creating safe and effective child medication, from initial research principles to real-world pharmaceutical applications, offering essential insights for professionals and researchers in the field.

Explore the intricate relationship between chemistry and drug development, with a specific focus on antibiotics. Understand the chemical synthesis, properties, and mechanisms of action for these vital pharmaceutical compounds used in healthcare.

This ACS symposium series explores the critical advancements in therapeutic protein and peptide formulation and delivery. It covers innovative strategies for enhancing stability, bioavailability, and targeted delivery of biopharmaceuticals, addressing challenges in drug development and paving the way for more effective and accessible protein and peptide-based therapies.

Download your Free Handbook of Pharmaceutical Excipients 7th Edition today! This essential guide provides comprehensive, up-to-date information on drug formulation excipients, crucial for professionals in pharmaceutical development and quality control.