About the Book
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 112. Chapters: Tablet, Spray drying, Clinical trial, Verification and validation, Effect size, Pharmaceutical marketing, Generic drug, Drug discovery, Product recall, Counterfeit medications, 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, Blister pack, NIPTE, Cold chain, Good Documentation Practice, Excipient, Good manufacturing practice, New Drug Application, Industrial biotechnology, In silico, Package insert, Contract research organization, 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, Vetter Pharma, Dry sterilisation process, Marketing authorization, Newhouse Research Site, International Society for Pharmaceutical Engineering, Track & Trace, Disease mongering, Assay sensitivity, Insulated shipping container, European Brain Council, Pharmaceutical lobby, Authorized generics, Drug repositioning, Drug discovery hit to lead, Downstream processing, Epedigree, Adverse event, Scrip World Pharmaceutical News, Moisture vapor transmission rate, ClinLife, Serious adverse event, General Practice Research Database, List of contract research organizations, Dublin Molecular Medicine Centre, Corrective and preventive action, Certificate of pharmaceutical product, Pre-clinical development, Drug Industry Document Archive, Inverse benefit law, Good Automated Manufacturing Practice, Healthy Skepticism, Good Clinical Practice, EUCOPE, Clinical trials unit, Contract manufacturing organization, Co-Pay Cards, Biologue, Medicines and Healthcare products...
