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Read the PharmaReady case study submitted by Conatus Pharmaceuticals.
Read the PharmaReady case study submitted by Dabur Pharma Limited

TAKE Solutions’ Life Sciences Division Announces Global Expansion of its Submissions Assurance™ Program (more)
TAKE Solutions’ Team Announces Conatus Pharmaceuticals the Winner in PharmaReady Best Case Study Contest (more)
New eCTD Submission Created Using PharmaReady 4.0 Passes FDA Validation (more)
When Sangart chose to adopt PharmaReady as its FDA-compliant document management solution, we knew that the ROI would be huge. What we didn’t quite anticipate was the overwhelming 'user acceptance' that the application has enjoyed — particularly among staff that had previous experience with very large competitive DMS brands."
Ford Winslow, Director, Information Systems
Sangart, Inc
"The PharmaReady product came at the perfect time for Wake Forest. With our confidence in the power of Microsoft's SharePoint™ Portal Server, PharmaReady successfully demonstrated how to achieve full management of SOPs, work instructions, and other documents regulated by the FDA - easily - and affordably. With the PharmaReady team’s knowledge and experience in both clinical research and information technology makes them an ideal business partner for Wake Forest. Any organization that's currently under-going a study to select an enterprise document management system should give PharmaReady careful consideration."
Scott Rushing, Deputy Director of Biostatistics
Wake Forest University Baptist Medical Center
"I have been monitoring the progress of our PharmaReady project very closely and have been able to personally work with your system. We have been very happy with the progress and have appreciated the attention you have given Synarc as a customer. We are looking forward to expanding our relationship and to using your software in other areas of the company."
Peter Steiger, Ph.D., CEO
Synarc
"At INC Research we chose PharmaReady as our Document Management System for handling electronic documents that fall within the scope of FDA's, and other regulators', electronic records and signature requirements. PharmaReady provides INC Research a cost-effective means to meet our stringent document management needs, and delivered the solution in a timely manner. The functionality of the web-based application allows us quick and easy access to our documentation from anywhere in the world.”
Vicky Green, Director, Global Clinical Applications
INC Research
"Our investigation found PharmaReady to be the most affordable document management solution on the market today. And the fact that PharmaReady meets the Federal regulations mandating Part 11, cGMP, and HIPAA compliance was key in our decision to select the PharmaReady solution."
David Gardner, President
ProviderLink
"InterDoc has been a leader in the Canadian pharmaceutical industry for many years. The PharmaReady solution has greatly enhanced our offering to customers looking to become 21 CFR Part 11 compliant but who are unable to afford a complex and expensive enterprise solution. Using the PharmaReady proven solution, along with our expertise in consulting, integration and custom development, will allow smaller companies to achieve compliance while maximizing their investment."
Danny Boulanger, President and CEO
InterDoc
"With PharmaReady, TAKE Solutions is well-positioned to successfully address the industry's demand for an EDMS that is robust, reliable and cost-effective. Using flexible, proven technology from Microsoft, this new offering helps the life sciences organizations improve business efficiencies and compliance readiness through enhanced communication and collaboration, across the enterprise’s regulated environment."
Steve Chin, Global Industry Manager, Life Sciences
Microsoft Corporation
"PharmaReady has the strategies needed to overcome challenges of using the Internet for clinical trials. If you're developing clinical systems, you must be closely aligned with partners that understand and have experience in this complex regulated environment. Designing, building and deploying validatable systems in the pharmaceutical arena is a core strength of PharmaReady."
Mark Paul, Director of eClinical Product Development
Quintiles Transnational