EthosExcel™ has listed a number of resources found on the internet here for your convenience. We feel these resources can be particularly useful for prospective or current Principal Investigators or those considering a career in clinical research.
Clinical Trials Information:
http://www.clinicaltrials.gov
US Office of Human Subject Research Protections (OHRP):
http://www.hhs.gov/ohrp/about
Clinical Research Standards:
http://www.cc.nih.gov/ccc/clinicalresearch/standards1.html
Convention of Human Rights and Biomedecine - Council of Europe (Spain, April 4, 1997):
http://conventions.coe.int/treaty/en/treaties/html/164.htm
Data Safety Monitoring for Phase I and II Trials:
http://grants.nih.gov/grants/guide/notice-files/NOT-OD-00-038.html
FDA:
http://www.fda.gov
FDA Regulations Relating to Good Clinical Practice and Clinical Trials:
http://www.fda.gov/ScienceResearch/SpecialTopics/RunningClinicalTrials/ucm114928.htm
FDA Guidance Documents:
http://www.fda.gov/RegulatoryInformation/Guidances/default.htm
Human Subjects Protections, 21 CFR 50:
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRsearch.cfm?CFRPart=50
Investigational Drugs, 21 CFR 312:
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCFR/CFRSearch.cfm?CFRPart=312
Subpart D--Responsibilities of Sponsors and Investigators
- 312.50 - General responsibilities of sponsors.
- 312.52 - Transfer of obligations to a contract research organization.
- 312.53 - Selecting investigators and monitors.
- 312.54 - Emergency research under 50.24 of this chapter.
- 312.55 - Informing investigators.
- 312.56 - Review of ongoing investigations.
- 312.57 - Recordkeeping and record retention.
- 312.58 - Inspection of sponsor's records and reports.
- 312.59 - Disposition of unused supply of investigational drug.
- 312.60 - General responsibilities of investigators.
- 312.61 - Control of the investigational drug.
- 312.62 - Investigator recordkeeping and record retention.
- 312.64 - Investigator reports.
- 312.66 - Assurance of IRB review.
- 312.68 - Inspection of investigator's records and reports.
- 312.69 - Handling of controlled substances.
- 312.70 - Disqualification of a clinical investigator.
- Association of Clinical Research Professionals (ACRP): www.acrpnet.org
- Drug Information Association (DIA): www.diahome.org
- Society of Clinical Research Associates (SOCRA): www.socra.org
- Applied Clinical Trials (on-line publication): www.actmagazine.com/appliedclinicaltrials
Date
Conferences & Meetings
Location
6/25/2013
Women's Business Enterprise National Council (WBENC) 2013 National Conference & Business Fair Read More >
Minneapolis, MN