About the Book
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 164. Chapters: Pharmaceutical industry, Pharmaceutical statistics, Pharmacodynamics, Pharmacokinetics, Blood-brain barrier, Tablet, Spray drying, Clinical trial, Verification and validation, Cytochrome P450, Effect size, Pharmaceutical marketing, Generic drug, Drug discovery, Product recall, Counterfeit medications, Porous silicon, Bioavailability, GoBalto, Inc., CenterWatch, Clinical research coordinator, Patient recruitment, Spheronisation, European Medicines Agency, Clinical trials registry, Clinical trial management, Pharmaceutical industry in the United Kingdom, Clinical monitoring, Clearance, Blister pack, NIPTE, Cold chain, Good Documentation Practice, Excipient, PEGylation, Good manufacturing practice, Biological half-life, New Drug Application, Industrial biotechnology, In silico, Package insert, Contract research organization, Physiologically based pharmacokinetic modelling, Capsule, Biopharmaceutical, Haim Aviv, Title 21 CFR Part 11, InnoMed PredTox, Centre for Molecular Medicine and Therapeutics, Cytel, Drug development, Black box warning, First DataBank, Process analytical technology, Industrial fermentation, Caco-2, Bioequivalence, Vetter Pharma, Dry sterilisation process, Marketing authorization, ADME, Absorption, Newhouse Research Site, International Society for Pharmaceutical Engineering, Tachyphylaxis, IC50, Plasma protein binding, Binding potential, Track & Trace, Disease mongering, Drug action, Assay sensitivity, Insulated shipping container, European Brain Council, Pharmaceutical lobby, Authorized generics, Drug repositioning, Drug discovery hit to lead, William E. Evans, Downstream processing, Epedigree, Microdosing, Adverse event, PAMPA, Scrip World Pharmaceutical News, Moisture vapor transmission rate, ClinLife, Serious adverse event, General Practice Research Database, List of contract research organizati...
