Policy: NIH plans to enhance reproducibility
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There is currently an absence of a culture of enhancing standards for environmental control, monitoring, and reporting in biomedical research.
“The task of enhancing standards for environmental control, monitoring, and reporting in biomedical research may initially seem overwhelming provided the current absence of a culture to this end (Collins and Tabak, 2014; Baker, 2016; Hunter, 2017).”
From Toward Best Practices for Controlling Mammalian Cell Culture Environments (2022) · cites this paper as Collins and Tabak, 2014
The Abstract says basic experimental-design details often go unreported, and PRECLINICAL PROBLEMS identifies different lab environments as a cause of irreproducible results. The paper calls for changes across the research community, but it does not specifically describe an absence of a culture of environmental control, monitoring, and reporting. Page numbers are unavailable in our copy. (LLM, conf=0.84)
Experimental — accuracy not yet measuredInability to reproduce study results, often inherent in observations from academic laboratories, is usually uncovered with relevant delay, e.g., when potential therapies transition from preclinical testing to clinical trials.
“The inability to reproduce study results, often inherent in observations from academic laboratories, are usually uncovered not without relevant delay, e.g. when potential therapies that are based on these findings transition from preclinical testing to the far more stringent conditions of clinical trials (Collins and Tabak, 2014).”
From In Vitro research Reproducibility: Keeping up High Standards (2019) · cites this paper as Collins and Tabak, 2014
The PRECLINICAL PROBLEMS section says preclinical research is particularly susceptible to irreproducible results, while clinical trials have more rigorous design and oversight. The PROPOSED NIH ACTIONS section discusses independently validating questionable animal-model findings before a clinical trial. Neither section says failures are usually discovered only after a substantial delay, when therapies enter clinical trials. (LLM, conf=0.83)
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- Authors
- Collins, F. S., & Tabak, L. A.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Tabak, Lawrence A.
- Venue
- Nature
- Published
- 2014-01-27
- Volume
- 505
- Issue
- 7485
- Pages
- 612-613
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4058759
- OpenAlex
- W2048060485
- Cited by
- 1,247
- References
- 8
- Citations by year
- 2026: 23 · 2025: 36 · 2024: 48 · 2023: 86 · 2022: 62 · 2021: 105 · 2020: 91 · 2019: 117 · 2018: 124 · 2017: 148 · 2016: 167 · 2015: 154 · 2014: 82 · 2012: 1
- FWCI
- 344.69
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health (Z99 OD999999)
- Topics
- Social Sciences › Decision Sciences › Information Systems and Management › Academic Publishing and Open Access
- Health Sciences › Veterinary › Small Animals › Animal testing and alternatives
- Social Sciences › Decision Sciences › Information Systems and Management › Research, Science, and Academia
- Keywords
- research reproducibility, National Institutes of Health, preclinical research, research integrity, scientific self-correction, science policy
- MeSH terms
- Animals, Female, Humans, Male, National Institutes of Health (U.S.), Pilot Projects, Research Design, Sex Characteristics, United States, Reproducibility of Results, Scientific Misconduct, Access to Information, Disclosure, Biomedical Research
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