Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Tom Brody"'
Autor:
Tom Brody
Clinical Trials: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines is a practical guidebook for those engaged in clinical trial design. This book details the organizations and content of clinical trials, including trial
Obtaining high-quality biopsy specimens is crucial for accurate diagnosis and treatment planning. The SuperCoreAdvantage™side notch semi-automatic biopsy device, developed by Argon Medical Devices, is a novel side notch semi-automatic biopsy device
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::380115ca4551abaecda4f38a3c302145
https://doi.org/10.14293/p2199-8442.1.sop-.pogx33.v1
https://doi.org/10.14293/p2199-8442.1.sop-.pogx33.v1
Artificial intelligence (AI) has shown potential in various aspects of healthcare, including medical education. This study explores the benefits and challenges of using AI-based tools, such as ChatGPT, in the training of medical students and interven
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfa941a428511cfe2bcd0baf8d64d7d8
https://doi.org/10.14293/p2199-8442.1.sop-.pftabj.v1
https://doi.org/10.14293/p2199-8442.1.sop-.pftabj.v1
Simulation training has played an important role in developing the hand eye coordination and basic procedural skill sets necessary to perform invasive procedures in multiple procedural specialties such as interventional cardiology, general surgery, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2d34d90d16e5e8a0f481e2099ec74b7
https://doi.org/10.14293/s2199-1006.1.sor-.pprkqbp.v1
https://doi.org/10.14293/s2199-1006.1.sor-.pprkqbp.v1
Autor:
Tom Brody
Nutritional Biochemistry takes a scientific approach to nutrition. It covers not just'whats'--nutritional requirements--but why they are required for human health, by describing their function at the cellular and molecular level. Each case study eith
Autor:
Tom Brody
Adjudication is used when the Sponsor of a new type of drug is faced with difficulty in deciding if one or more adverse events occurring in patients during the course of a clinical trial are related, or are not related, to the study drug. Adjudicatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91f598de0ba7a379cc37bf032e75856c
https://doi.org/10.1016/b978-0-12-814647-7.00012-9
https://doi.org/10.1016/b978-0-12-814647-7.00012-9
Autor:
Tom Brody
Most of the package labels for any drug consist of warnings about toxicity. Toxicity in humans is also known as “adverse events.” But some package labels have special instructions for increasing the dose or decreasing the dose, when special circu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4e6db7d25795642d8182319c3fa71b5
https://doi.org/10.1016/b978-0-12-814647-7.00004-x
https://doi.org/10.1016/b978-0-12-814647-7.00004-x
Autor:
Tom Brody
This chapter summarizes many of the take-home lessons from this entire book. This chapter provides excerpts from FDA’s reviews from 100 different drugs. This book is based on the author’s reading of data from 100 of FDA’s reviews for 100 differ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b6dc94d2e1bcaa01495c34754191199
https://doi.org/10.1016/b978-0-12-814647-7.00002-6
https://doi.org/10.1016/b978-0-12-814647-7.00002-6