Leading provider of teleseminars and webinars based on quality assurance, regulatory compliance and clinical to the Medical Device, Pharmaceutical and Food industries. We provide high-quality and high-value sessions with industry experts for our clients.
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FDAteleseminars.com - Home | fdateleseminars.com Reviews
https://fdateleseminars.com
Leading provider of teleseminars and webinars based on quality assurance, regulatory compliance and clinical to the Medical Device, Pharmaceutical and Food industries. We provide high-quality and high-value sessions with industry experts for our clients.
fdateleseminars.com
FDAteleseminars.com - Pricing/Payment
http://www.fdateleseminars.com/Pricing-Payment.html
The expert regulatory discussion sessions company. Pricing and Payment Information. Group rates* (5 attendees) - Please inquire. More Attendees : Please inquire. Recording only - MP3 downloads (CD's will be mailed upon request). To register for additional attendee's call (952) 405-9093 or. Group registrations include unlimited log-ins. A separate log-in for each attendee will be provided at no. Or contact us form we will be happy to assist you. You for choosing FDA Teleseminars. Join the mailing list.
FDAteleseminars.com - About us
http://www.fdateleseminars.com/About-us.html
The expert regulatory discussion sessions company. And webinars based on. Quality assurance, FDA regulatory compliance and clinical to the Medical Device, Pharmaceutical and Food industries. We provide clients with high-quality and high-value sessions with industry experts.W e are committed to meeting the needs of our clients by providing unbiased guidance and advice. Teleseminars or teleconferencing and webinars provide a way to bring people together effectively and inexpensively. Content is a key ,.
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The expert regulatory discussion sessions company. Join the mailing list. 5115 Excelsior Blvd, # 418, St Louis Park,Minnesota- 55416.
FDAteleseminars.com - Informed Consent
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The expert regulatory discussion sessions company. Informed Consent" structure and guidelines according IRB's, NIH-HRPP, FDA, HIPAA. Wednesday, March 31st, 2010. Virgilio Vinas, MD, MPH, PhD. What Is Informed Consent? Informed consent is essential to research ethics. The informed consent is defined as:. Consent given by a competent individual who:. Has received the necessary information(Verbally and in Writing). Has adequeately understood the information. Informed Consent as a Process. About the speaker :.
FDAteleseminars.com - Preparation for a FDA Audit
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The expert regulatory discussion sessions company. Preparation for an FDA Audit. May 12th, 2010. Robert Schiff, PhD, RAC, CQA. About the Speaker :. Robert Schiff, PhD, RAC, CQA, is founder and CEO of Schiff and Company, a. Ffairs, Compliance and Clinical Research Organization, established in 1982. Prior to founding Schiff and Company, Dr. Schiff served with a number of companies including:. Dr Schiff has authored over 50 publications and holds several patents on medical products. College of New York.
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The expert regulatory discussion sessions company. FDA regulatory teleseminar and webinar company. Which showcases the opinion of. Industry experts through regular seminars/sessions. Quality assurance,clinical, and regulatory compliance. To the Medical Device, Pharmaceutical and Biotech industries. Provide high-quality and high-value sessions with industry experts for our clients. Software Quality Analysis, a. Preparation for an FDA Audit. Wed, May 12th, 2010. 12pm - 1pm EST. Robert Schiff, PhD, RAC, CQA.
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FDA THINK TANK
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