ClinfoSource @ClinfoSource
ClinfoSource provides online GCP Compliance training and certification programs for clinical trials under FDA regulations for the bio-pharmaceutical industry. clinfosource.com Danville, California Joined March 2012-
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ClinfoSource June 2013 Regulatory News for Clinical Trials Professionals - #FDA, #EMA, #HealthCanada update policies clinfosource.com/documents/repo…
I liked a @YouTube video from @ClinfoSource youtu.be/8e-Pxqasuo0?a ClinfoSource Demo - Safety Reporting in Clinical Trials
ClinfoSource provides latest FDA guidelines, regulations in online training programs for #ClinicalTrials research. clinfosource.com/documents/Repo…
ClinfoSource Regulatory News Report - December 2012: Top 7 topics for clinical research personnel. clinfosource.com/documents/Repo… #ClinicalTrials
ClinfoSource Regulatory News Report, November 2012: FDA publishes Draft Guidance in Federal Register. clinfosource.com/documents/Repo… #ClinicalTrials
#ClinfoSource Newsletter November 2012 -- New online GCP training course for Medical Device Monitoring #ClinicalTrials bit.ly/MedicalDeviceT…
ClinfoSource Announces Online GCP Training Program for Medical Device Trials - eepurl.com/rrFZz
Making a difference every day... the work of PhD Cand. Marlien Varnfield and her colleagues. Marlien Varnfield... fb.me/1h7jGcdrY
Indian Regulators release new regulations governing clinical trials and "Order & Notice for Informed Consent" clinfosource.com/documents/EMA-…
Ed Markey's Trial & Experimental Studies Transparency (TEST) Act of 2012 to further protect humans in #clinicaltrials clinfosource.com/documents/EMA-…
Must-Know: "Annual report of the Good Clinical Practice Inspectors Working Group 2011", adopted by GCP IWG, 23 May 2012 ema.europa.eu/docs/en_GB/doc…
EMA replaces 2001 Clinical Trials Directive with July 2012 Clinical Trials Regulation. Easier clinical trials in EU. clinfosource.com/documents/EMA-…
ClinfoSource and Quintiles Transnational Sign Licensing Agreement for Clinical Research Training prweb.com/releases/2007/…
Infinity Pharma Stops Phase 2 #ClinicalTrials of Saridegib as treatment shows similar to placebo: fiercebiotech.com/press-releases… #BioPharma
GCP #ClinicalTrials training topics "Informed Consent" teach "Elements & Documentation" and "Process & Exceptions" http://bit.ly/Clinfo1
Training module "Investigator Responsibilities" for #ClinicalTrials human subject rights, safety, and welfare for IRB. clinfosource.com/catalog/lp_bro…
FDA Clinical Trials Guidance Documents represent view on good clinical practice (GCP) and conduct of clinical trials. fda.gov/RegulatoryInfo…

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