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Explore essential principles of Good Clinical Practice for conducting ethical, safe clinical trials. Learn key concepts, guidelines, and regulatory requirements to ensure data integrity in pharmaceutical research.
Comprehensive guide to patient recruitment, consent processes, and trial conduct in clinical research, emphasizing GCP compliance and ethical considerations for diverse patient groups.
Comprehensive introduction to clinical trial preparation, focusing on investigator qualifications, site selection, essential documents, ethics committees, and roles of investigators and site staff.
Comprehensive overview of preclinical drug discovery, from target identification to clinical trials, for life scientists and professionals in related fields. Covers key processes, challenges, and strategies.
Comprehensive exploration of pharmacokinetics, covering ADME, PK parameters, in vitro assays, and PK/PD relationships. Suitable for life scientists and professionals in drug discovery-related fields.
Explore the development of active compounds into suitable formulations for animal studies and early clinical trials, covering key factors in drug design and administration.
Explore in vitro and in vivo toxicology studies, safety risk assessments, and human dose selection in drug discovery, emphasizing patient safety and therapeutic index determination.
Explore drug discovery stages, focusing on lead identification and optimization. Learn about screening assays, selection criteria, and structure-activity relationships through an antimalarial therapy case study.
Explore early drug discovery stages, focusing on assays and screening methods to identify promising compounds. Learn about target engagement validation and different approaches in pharmaceutical research.
Explore the complex process of preclinical drug discovery, from target identification to pre-formulation, in this comprehensive specialization designed for graduate-level life sciences professionals.
Equip yourself with essential knowledge for conducting reliable and ethical clinical trials, ensuring participant safety, data integrity, and compliance with international regulations.
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