Literature DB >> 21731522

Clinical investigator responsibilities.

Allison R Baer1, Susan Devine, Chris David Beardmore, Robert Catalano.   

Abstract

When conducting a clinical trial, it is important that clinical investigators successfully meet all research expectations, including regulatory requirements and the Guidelines for Good Clinical Practice.

Year:  2011        PMID: 21731522      PMCID: PMC3051859          DOI: 10.1200/JOP.2010.000216

Source DB:  PubMed          Journal:  J Oncol Pract        ISSN: 1554-7477            Impact factor:   3.840


  3 in total

1.  Responsibility of applicants for promoting objectivity in research for which public health service funding is sought and responsible prospective contractors. Final rule.

Authors: 
Journal:  Fed Regist       Date:  2011-08-25

2.  American Society of Clinical Oncology Statement on minimum standards and exemplary attributes of clinical trial sites.

Authors:  Robin Zon; Neal J Meropol; Robert B Catalano; Richard L Schilsky
Journal:  J Clin Oncol       Date:  2008-04-07       Impact factor: 44.544

3.  The Belmont Report. Ethical principles and guidelines for the protection of human subjects of research.

Authors: 
Journal:  J Am Coll Dent       Date:  2014
  3 in total
  5 in total

1.  The clinical research team.

Authors:  Allison R Baer; Robin Zon; Susan Devine; Alan P Lyss
Journal:  J Oncol Pract       Date:  2011-05       Impact factor: 3.840

Review 2.  Clinical Trials and the Role of the Oncology Clinical Trials Nurse.

Authors:  Elizabeth A Ness; Cheryl Royce
Journal:  Nurs Clin North Am       Date:  2017-03       Impact factor: 1.208

3.  Application of Incident Command Structure to clinical trial management in the academic setting: principles and lessons learned.

Authors:  Penny S Reynolds; Mary J Michael; Bruce D Spiess
Journal:  Trials       Date:  2017-02-09       Impact factor: 2.279

4.  Effect of a planned training session on good clinical practice knowledge in research professionals: A pilot study.

Authors:  Kasturi Awatagiri; Durga Gadgil; Sadhana Kannan; Pallavi Rane; Bhavesh Bandekar; Nilam Sawant; Prafulla Parikh; Vedang Murthy
Journal:  Perspect Clin Res       Date:  2019 Jan-Mar

5.  Informed consent procedure in a double blind randomized anthelminthic trial on Pemba Island, Tanzania: do pamphlet and information session increase caregivers knowledge?

Authors:  Marta S Palmeirim; Amanda Ross; Brigit Obrist; Ulfat A Mohammed; Shaali M Ame; Said M Ali; Jennifer Keiser
Journal:  BMC Med Ethics       Date:  2020-01-06       Impact factor: 2.652

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.