• Zamawiaj do paczkomatu
  • Płać wygodnie
  • Obniżka
Oxford Handbook of Clinical and Healthcare Research

Oxford Handbook of Clinical and Healthcare Research

9780199608478
252,65 zł
227,38 zł Zniżka 25,27 zł Brutto
Najniższa cena w okresie 30 dni przed promocją: 227,38 zł
Ilość
Od 4 do 6 tygodni

  Dostawa

Wybierz Paczkomat Inpost, Orlen Paczkę, DPD, Pocztę, email (dla ebooków). Kliknij po więcej

  Płatność

Zapłać szybkim przelewem, kartą płatniczą lub za pobraniem. Kliknij po więcej szczegółów

  Zwroty

Jeżeli jesteś konsumentem możesz zwrócić towar w ciągu 14 dni*. Kliknij po więcej szczegółów

Opis
The Oxford Handbook of Clinical and Healthcare Research is an evidence-based, succinct, and easy-to-use reference for the full range of clinical and healthcare research topics. Providing a wide breadth of essential knowledge, this comprehensive text takes the researcher through the steps from general good clinical practice in healthcare research to the process and management of research. This handbook includes clear instructions on the legislative and practical requirements of commissioning, conducting, analysing, and reporting research for those in clinical or healthcare practice, education, or training. Written with Good Clinical Practice (GCP) education in mind, it includes valuable information needed for the accredited certificates and diploma-level benchmark exams now commonly required by employers. This is a definitive text for all clinical and healthcare researchstudents, as well as graduates with an interest in clinical and healthcare research.
Szczegóły produktu
OUP Oxford
86836
9780199608478
9780199608478

Opis

Rok wydania
2016
Numer wydania
1
Oprawa
miękka foliowana
Liczba stron
608
Wymiary (mm)
100 x 180
Waga (g)
322
  • Research - How and Why; Basic concepts in biostatistics and epidemiology; Quantitative and clinical / epidemiological methods; Qualitative methods; Evidence Based Medicine (EBM); Critical appraisal; Clinical Audit; Setting the scene and ICH-GCP in clinical and healthcare research; Informed consent in a research setting; Ethics of clinical and healthcare research: general considerations, Mental Capacity Act, Human Tissue Act; Role and Responsibilities: Investigators and Research Team; Role and Responsibilities: Sponsor; Monitoring; Clinical Trial Design; Clinical Trial Protocols: Study Protocol; Data Capture Tools: Case Report Form (CRF); Clinical Trial Supplies: IMPs; IMP Accountability; Safety Reporting; Data management; Research Project Management; Essential Documents; Archiving; Audits and Inspections; Fraud and Misconduct; Authorship; Publication process; Start-up toolkit: from funding an idea, through implementation, to achieving an impact;
Komentarze (0)