Carey Smoak

See the following -

Clinovo White Papers Published In Summer 2014 Editions Of Leading Medical Device & Pharmaceutical Publications

Press Release | Clinovo | July 29, 2014

White papers by Clinovo on CDISC Standards for medical devices and cloud-based eClinical technologies have been published in the latest editions of leading pharmaceutical publications Data Basics and Med Device Online...

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CDISC for Medical Device Companies: Progress Made and Best Practices from Pharma/Biotech Implementation

Event Details
Open Source Event
October 9, 2013 - 6:30pm - 9:00pm
Capgemini Offices, South San Francisco
20425 Stevens Creek Blvd
Cupertino, CA 95014
United States

The healthcare industry, as well as regulatory bodies, have been hard at work in the standardization of clinical trial data. The need for data transparency, traceability, and auditability has continued to increase, in line with the cost of studies and the amount of data submitted to the FDA. As a result, much progress has been made in the past decade in creating standards to ease data exchange and interoperability as well as speed up the regulatory review process.

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