The experts resource for Clinical Research Audit training. GCP Training, Clinical Quality Assurance Training, GCP, FDA, IRB. Training by field experienced experts
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Kent Associates, Inc.
Phyllis Kent
61 Cle●●●●●●d Road
Cal●●●ell , New Jersey, 07006-5727
United States
View this contact
Kent Associates, Inc.
Phyllis Kent
61 Cle●●●●●●d Road
Cal●●●ell , New Jersey, 07006-5727
United States
View this contact
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Quality Research Training Institute | GCP Training | GCP FDA IRB Training | qrti.com Reviews
https://qrti.com
The experts resource for Clinical Research Audit training. GCP Training, Clinical Quality Assurance Training, GCP, FDA, IRB. Training by field experienced experts
qrti.com
About Us | Quality Research Training Institute | Clinical Research Audit Training | GCP FDA IRB Training
http://www.qrti.com/about_us.php
Our Founders, The Expert's Experts. Rochelle L. Goodson. 1010 0011 1101 1111 0101 1100 0001 0100. Phyllis B. Kent. 1010 0011 1101 1111 0101 1100 0001 0100.
Quality Research Training Institute | Online Training | GCP FDA IRB Training
http://www.qrti.com/webinars.php
Thursday September 1, 2016. Registration must be received 3 business days prior to the event date. You must notify us of any cancellation at least 3 business days prior to the scheduled event to receive a credit. We reserve the right to cancel any seminar not meeting minimum enrollment. The Clinical Research Quality Assurance Expert's Expert Source. The Quality Research Training Institute. Caldwell, NJ 07006-5727. Telephone: 516-374-5858 or 973-226-4679. The First Friday of Every Month.
Quality Research Training Institute | Clinical Research Audit Training | GCP FDA IRB Training
http://www.qrti.com/training_managers.php
Thursday September 1, 2016. FDA guidance on transferring oversight to another IRB. FDA guidance on responsibilites related to informed consent. FDA guidance on electronic media and informed consent. FDA guidance on conducting medical device clinical trials. FDA guidance on acceptance of medical device clinical data. Guidance for Industry: Oversight of Clinical Investigations - A Risk-Based Approach to Monitoring. The Clinical Research Quality Assurance Expert's Expert Source. Are you responsible for:.
Quality Research Training Institute | Clinical Research Audit Training | GCP FDA IRB Training
http://www.qrti.com/resources.php
Thursday September 1, 2016. FDA IRB Registration Rule. Study data may be fake. Biosearch Moniotring Information System (BMIS) File. New FDA Policy Strengthening the Regulation of Clinical Trials and Bioresearch Monitoring. Clinical Study Coordinator for Pediatric Drug Sentenced for Fraud. Allegations of Fake Research Hit New High. Critics see flaws in Drug-Safety Monitoring. Neuroscientist censured for misconduct. Death Points to Risks in Research. Scientific fraud' hampered spread of cancer technique.
Quality Research Training Institute | GCP Training | GCP FDA IRB Training
http://www.qrti.com/index.php
Thursday September 1, 2016. FDA guidance on transferring oversight to another IRB. FDA guidance on responsibilites related to informed consent. FDA guidance on electronic media and informed consent. FDA guidance on conducting medical device clinical trials. FDA guidance on acceptance of medical device clinical data. Guidance for Industry: Oversight of Clinical Investigations - A Risk-Based Approach to Monitoring. The Clinical Research Quality Assurance Expert's Expert Source.
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Thursday August 13, 2015. FDA guidance on transferring oversight to another IRB. FDA guidance on responsibilites related to informed consent. FDA guidance on electronic media and informed consent. FDA guidance on conducting medical device clinical trials. FDA guidance on acceptance of medical device clinical data. Guidance for Industry: Oversight of Clinical Investigations - A Risk-Based Approach to Monitoring. The Clinical Research Quality Assurance Expert's Expert Source.
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