dr.pierce1.net
PIERCE ONE CONSULTING- Research subject / patient safety, Investigator GCP training
http://dr.pierce1.net/resources.html
Charles H. Pierce, MSc, MD, PhD, FCP, CPI. Consultant in Pharmaceutical and Medical Research. Pierce One, Consulting. Charles H. Pierce, MD, PhD. Cincinnati, Ohio 45239. Importance of Data Safety Monitoring-65. Usefulness of 21 CFR Part 11 in Clinical Research. Curriculum Vitae, CH Pierce. Professional Biography, CH Pierce. The Art and Science of Presenting. Use of Half-Life Information. CPU Requirements TOC - Mar08. Global Clinical Partners, Inc. Association of Clinical Pharmacology Units. This web site...
salusirb.com
IRB Information & Resources on Human Subjects in Research
https://www.salusirb.com/resources
Administering Informed Consent (Form 640). Recruitment and Study Material (Form 610). Electronic Records/Electronic Signatures 21 CFR 11. Financial Disclosure by Clinical Investigators 21 CFR 54. Good Clinical Practice and Clinical Trials. Institutional Review Boards 21 CFR 56. Investigational Device Exemption (IDE) 21 CFR 812. Investigational New Drug (IND) 21 CFR 312. Premarket Approval of Devices 21 CFR 814. Protection of Human Subjects 21 CFR 50. Device Advice: Comprehensive Regulatory Assistance.
bchrs.com
Who We Are - BCH Research Solutions
http://www.bchrs.com/who-we-are.html
Clinical Trial Consulting and Monitoring. Medical Writing for Regulatory Submission. BCH Research Solutions, LLC. Expert Clinical Research, Medical Writing and Consulting Services. We believe in sustained business relationships with our clients. Our clients, who range from biotech start-ups to the global life sciences companies, are engaged in the development of new pharmaceutical and biological products and vaccines. Our Professional Membership Organizations. Drug Information Association (DIA).
clinpharmnetwork.com
ClinPharm Network - Evaluation & Audit
http://clinpharmnetwork.com/pages/consulting-services/evaluation-audit.php
SOP and Process Improvement. Ensuring GCP Standards Excellence. By increasing the amount of accurate and reliable data Sponsors have about clinical facilities, the ClinPharm Network (CPN) helps to match quality providers with the right projects to shorten the time and reduce the costs involved in the launch of new studies. Click here to learn more about the CPN audit and evaluation process. Ldquo;Adherence to the principles of good clinical practices (GCPs), including adequate human subject protection (H...
salusirb.com
Resources | Salus IRB
https://www.salusirb.com/getting-started/resources
Administering Informed Consent (Form 640). Recruitment and Study Material (Form 610). Electronic Records/Electronic Signatures 21 CFR 11. Financial Disclosure by Clinical Investigators 21 CFR 54. Good Clinical Practice and Clinical Trials. Institutional Review Boards 21 CFR 56. Investigational Device Exemption (IDE) 21 CFR 812. Investigational New Drug (IND) 21 CFR 312. Premarket Approval of Devices 21 CFR 814. Protection of Human Subjects 21 CFR 50. Device Advice: Comprehensive Regulatory Assistance.
larc.net
Clients - Laura A. Robbins Consulting, LLC
http://larc.net/clients
Laura A. Robbins Consulting, LLC. American Federation for Aging Research. Asheville Symphony Orchestra Guild. The Association of Clinical Pharmacology Units. The Gerontological Society of America. John A. Hartford Foundation. United Way of New York City. University of Southern California. Visiting Nurse Service of New York. Arden, NC 28704.
verifiedclinicaltrials.com
Dual Enrollment In Clinical Trials & Professional Research Subjects Causing Increased Placebo Rates: Visit Verified Clinical Trials At Outsourcing Meeting New England October 7th, 2014 - Verified Clinical Trials
http://www.verifiedclinicaltrials.com/dualenrollmentclinicaltrials+Outsourcing+New+England
Call Us Today: 1-516-998-7499. Latest News and History. Facts & Figures. Dual Enrollment In Clinical Trials & Professional Research Subjects Causing Increased Placebo Rates: Visit Verified Clinical Trials At Outsourcing Meeting New England October 7th, 2014. VCT), the global research subject clinical trials database registry. Dual enrollment in clinical research trial. Will be attending and exhibiting at the Outsourcing In Clinical Trials New England. Is dedicated to reducing protocol violations. From en...
