PIDB – Clinical Data Provider

Written by Global_PM_Systems Posted on Wednesday, December 4, 2013 No Comments

What is really exciting about this week???

GPMS has now entered into a different channel as a Solution Provider. Traditionally, we have been a services company. In more recent years, we became a VAR (Value Added Reseller) and added various PPM products to our portfolio. With the organic development of the Principal Investigator Database Suite (PIDB), we are launching an entirely different suite of IT solutions to our clients. PIDB is a Data Service Provider, which allows clients to employ their

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DICE – License Eligibility

Written by Global_PM_Systems Posted on Friday, November 8, 2013 No Comments

It’s hard enough to find a Clinical Investigator for your Clinical Trial but then to find one without any infractions makes it even harder. The challenge is not finding a practitioner without infractions; the challenge is the ability to validate the license eligibility of the practitioner. Many organizations today want to automate and simplify the entire Study Site Startup process but struggle in these areas due to lack of technology and accurate data. It’s hard to imagine today that information

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DICE – Debarments, Inspections, Compliance and Enforcements for Clinical Trials.

Written by Global_PM_Systems Posted on Wednesday, October 23, 2013 No Comments

Today, Sponsors have a growing concern about the selection of the Clinical Investigator during recruitment. As many pharma and healthcare companies outsource the entire clinical trial to CRO’s , the expectation is that the CRO’s have been diligent in their selection of an investigator in that the investigator is experienced in the field and has a clean record of trial performance. As there are many areas of concern during Study Site Startup (‘SSSU’), compliance remains a key area for the

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