For more information or to register for the seminar, please click here (http://www.complianceonline.com/
Seminar instructor Glenda Guest is the vice president of Norwich Clinical Research (http://www.complianceonline.com/
As vendor oversight is an important sponsor obligation, regardless of the product being developed, laying the foundation for quality should begin during the vendor selection process. Unless the company clearly states the requirements in Request for Proposal (RFP) process, it can end up unable to make an ‘apple to apple’ comparison and may also select a substandard vendor. This seminar will explain how to save a clinical research team’s time by ensuring that the RFP process will produce results that enable comparison of vendors.
This course will be valuable for medical device and drug firm senior executives, directors, managers and those who have responsibility for outsourcing and vendor selection. It can also be beneficial for officials from clinical operations, vendor management, quality and compliance and project managers in the FDA regulated companies.
Date: Wednesday, February 20 (8.00 AM-4.00 PM) PDT and Thursday, February 21, 2013, (8.00 AM- 1.00 PM) PDT
Venue & Location: Grand Hyatt San Francisco
345 Stockton Street,
San Francisco, CA 94108
Registration Cost: $1,299.00 per registration
Early bird discounts: For discounts on early registrations, please click here.
Register by phone: Please call our customer service specialists at +1-650-620-3937 or email to customercare@
For more information on ComplianceOnline or to browse through our trainings, please visit our website (http://www.complianceonline.com/?
For more information please contact:
A Reuben Bernard
Manager of Program Marketing
2600 E Bayshore Rd
Palo Alto CA USA 94303