Principles and Practice of Clinical Research

Forfatter: info mangler
Bog
  • Format
  • Bog, hardback
  • Engelsk

Beskrivelse

Principles and Practice of Clinical Research, Fourth Edition has been thoroughly revised to provide a comprehensive look at both the fundamental principles and expanding practice of clinical research. New to this edition of this highly regarded reference, authors have focused on examples that broadly reflect clinical research on a global scale while including a discussion of international regulations, studies, and implications. In addition to key topics such as bioethics, clinical outcome data, cultural diversity, protocol guidelines, and “omic” platforms, this edition contains new chapters devoted to electronic health records and information resources for clinical researchers, as well as the many opportunities associated with big data. Covering a vast number of topics and practical advice for both novice and advanced clinical investigators, this book is a highly relevant and essential resource for all those involved in conducting research.

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Detaljer
  • SprogEngelsk
  • Sidetal824
  • Udgivelsesdato21-12-2017
  • ISBN139780128499054
  • Forlag Academic Press Inc
  • FormatHardback
Størrelse og vægt
  • Vægt2360 g
  • coffee cup img
    10 cm
    book img
    21,6 cm
    27,6 cm

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    Metadata Interview Power Law Drug History Media Ethics Education Clinical trials Data analysis Data collection Drug development Foundations Health policy Informed Consent. Information system Pregnant women Case Report Bibliometrics Competency-based education Quality of life Privacy Clinical pharmacology Philanthropy Medical errors Peer review Hypothesis Curriculum Accreditation Communications Evidence-based medicine Bioinformatics Measurement Pharmacogenomics Collection Cross-Sectional Studies Conflict of Interest Comparative Effectiveness Research Data management Global health Patient safety Clinical trial Quality Improvement Failure mode and effects analysis Invention Medical Record Linkage Health Equity patent Public Publication Bias Confidence interval Product development Grant writing Data Sharing Electronic medical record Cohort Metaanalysis International Conference on Harmonisation Missing data Performance measurement Grant funding License Log-rank test Challenges Masking Function Public health policy Biorepository Prepare Information Disclosure Opportunities Biomarkers Clinical research Nonparametric Diagnostic tests Harm Message Patient Reported Outcomes Health Informatics Kaplan Meier Audits Odds Ratio Heterogeneity Multiple Comparisons Database Linkage Biologics Ich Alpha-Level Correlation Censoring Electronic Health Record Allocation Case-control study Health-Related Quality of Life Adaptive designs Patient-Centered Effect size Causal inference Overhead EMR Efficacy Interim Analysis Health disparities Inclusion policy Null hypothesis P-value Metaregression Infringement Collaborations Common Rule NIH Funding Institutional Review Board Adaptive Randomization Adverse event reporting Alternative hypothesis Authorship and publication Bibliographic Databases Bibliographic file management Central IRBs Clinical research careers Career development awards Clinical data sets Clinical research nursing Bayh-Dole Clinical research data warehouse (CRDW)Clinical research data Career award Blinding (masking)Control groups Data and safety monitoring board (DSMB)Data quality Biologic licensing application Biospecimen Cox proportional hazards regression Clinical trial registration Drug regulatory harmonization case series EHR system architecture Controlled clinical trial Dissemination and implementation studies Certificates of confidentiality Citation Searching Clinical data repository Clinical research data repository (CRDR)EHR Clinical Research Protocol Clinician-scientists Clinical trials data management system ClinicalTrials.gov Exclusionary Criteria Fixed-effect model Explanatory versus pragmatic trials Data objectivity and subjectivity Data standards Hourly rate ICH harmonized tripartite guideline Grant review Human Subjects Protection Inclusionary criteria Intent-to-treat (ITT)Permuted block randomization Interim monitoring Human research protection program Dose ranging HRPP EMBASE Institutional review board (IRB)Research ethics equipoise International Classification of Function literature searching Nested study New drug application Methodology of clinical research Nursing certification Participant safety good clinical practice Grant opportunities Patient perceptions Per patient budget Hazard Function Human subject protections Pragmatic clinical trial Patient-scientist partnership Prevalence survey Human and animal research Institutional review boards Grant support Preanalytical variable Product Development Partnerships Protocol budget International Council on Harmonisation Internet-based resources Manual of operating procedures Mentor/mentee relationship Learning Health Care Systems Phase I-IV studies PubMed/Medline patient perspective Placebo responding Pseudorandomization AAHRPP

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