Detecting Data Quality Issues in Clinical Trials: Current Practices and Recommendations. (January 2016)
- Record Type:
- Journal Article
- Title:
- Detecting Data Quality Issues in Clinical Trials: Current Practices and Recommendations. (January 2016)
- Main Title:
- Detecting Data Quality Issues in Clinical Trials
- Authors:
- Knepper, David
Fenske, Christian
Nadolny, Patrick
Bedding, Alun
Gribkova, Elena
Polzer, John
Neumann, Jennifer
Wilson, Brett
Benedict, Joanne
Lawton, Andy - Abstract:
- Background: Data quality issues in clinical trials can be caused by a variety of behaviors including fraud, misconduct, intentional or unintentional noncompliance, and significant carelessness. Regardless of how these behaviors are defined, they may compromise the validity of the study results. Reliable study results and quality data are needed to evaluate products for marketing approval and for decisions that are made on the use of medicine. This article focuses on detecting data quality issues, irrespective of origin or motive. Early detection of data quality issues are important so that corrective actions taken can be implemented during the conduct of the trial, recurrence can be prevented, and data quality can be preserved. Methods: A survey was distributed to TransCelerate member companies to assess current strategies for detecting and mitigating risks involving fraud and misconduct in clinical trials. A review of literature across many industries from 1985 to 2014 was conducted using multiple platforms. Results: Eighteen TransCelerate member companies anonymously responded to the survey. All of the respondents had one or more existing strategies for fraud and misconduct detection. The literature search identified current practices and methodologies across many industries. Conclusions: TransCelerate recommends the creation of an integrated, multifaceted approach to proactively detect data quality issues. Detection methods should include a strategy tailored to theBackground: Data quality issues in clinical trials can be caused by a variety of behaviors including fraud, misconduct, intentional or unintentional noncompliance, and significant carelessness. Regardless of how these behaviors are defined, they may compromise the validity of the study results. Reliable study results and quality data are needed to evaluate products for marketing approval and for decisions that are made on the use of medicine. This article focuses on detecting data quality issues, irrespective of origin or motive. Early detection of data quality issues are important so that corrective actions taken can be implemented during the conduct of the trial, recurrence can be prevented, and data quality can be preserved. Methods: A survey was distributed to TransCelerate member companies to assess current strategies for detecting and mitigating risks involving fraud and misconduct in clinical trials. A review of literature across many industries from 1985 to 2014 was conducted using multiple platforms. Results: Eighteen TransCelerate member companies anonymously responded to the survey. All of the respondents had one or more existing strategies for fraud and misconduct detection. The literature search identified current practices and methodologies across many industries. Conclusions: TransCelerate recommends the creation of an integrated, multifaceted approach to proactively detect data quality issues. Detection methods should include a strategy tailored to the characteristics of the study. Some sponsors are taking advantage of more advanced methods and integrated processes and systems to proactively detect and address issues, relying on advances in technology to more efficiently review data in real time. Further research is underway to assess statistical data quality detection methodology in clinical trials. … (more)
- Is Part Of:
- Therapeutic innovation & regulatory science. Volume 50:Number 1(2016:Jan.)
- Journal:
- Therapeutic innovation & regulatory science
- Issue:
- Volume 50:Number 1(2016:Jan.)
- Issue Display:
- Volume 50, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 50
- Issue:
- 1
- Issue Sort Value:
- 2016-0050-0001-0000
- Page Start:
- 15
- Page End:
- 21
- Publication Date:
- 2016-01
- Subjects:
- good clinical practice -- risk-based monitoring -- centralized monitoring -- statistical monitoring -- risk indicators -- clinical trial fraud -- clinical trial misconduct
Drugs -- Periodicals
Pharmacology -- Periodicals
Drugs -- Research -- Periodicals
Drugs -- Testing -- Periodicals
615.1 - Journal URLs:
- http://dij.sagepub.com/ ↗
http://dij.sagepub.com/content/by/year ↗
http://journals.sagepub.com/toc/DIJ/current ↗
https://www.springer.com/journal/43441 ↗
http://www.sagepublications.com/ ↗ - DOI:
- 10.1177/2168479015620248 ↗
- Languages:
- English
- ISSNs:
- 2168-4790
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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