| Literature DB >> 34050748 |
Jonathan Kagan1, Geoffrey N Goodman2, Rachel Oh2, Diane Whitworth2, Darcie Gladden2, Gail Graves2, Antonia Nguyen2, Orish Shrestha2, Gerald Burge3, Mary Smolskis1, Janet Andrews4, Brian Cramer2, H Clifford Lane1.
Abstract
Regulatory compliance is challenging for multinational clinical trials. Conflicts between country requirements impedes research and slows the approval of medicines, leading the pharmaceutical industry to devote significant resources to this area. Many academic centers and nonprofits cannot support industry-level investment and are vulnerable to noncompliance. To address an insufficiency in public access to this information, the National Institute of Allergy and Infectious Diseases developed ClinRegs-a public access database of clinical research regulations. This report describes ClinRegs' features, maintenance, and usage. From September 2019 through August 2020, ClinRegs had 68 504 users, 60% from outside the United States, demonstrating the demand for accessible, reliable, country-specific regulatory information. Tools such as ClinRegs can help increase regulatory compliance and free up resources for research. We encourage our partner agencies and biomedical research industries to promote greater regulatory knowledge sharing and harmonization for the betterment of clinical research and improved public health. Published by Oxford University Press for the Infectious Diseases Society of America 2021.Entities:
Keywords: clinical research quality; clinical research regulations; clinical trial ethics; global clinical trials; public access
Mesh:
Year: 2021 PMID: 34050748 PMCID: PMC8492127 DOI: 10.1093/cid/ciab505
Source DB: PubMed Journal: Clin Infect Dis ISSN: 1058-4838 Impact factor: 20.999