Client Testimonials
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"TAKE Solutions came in at the perfect time for Wake Forest. With our confidence in the power of Microsoft’s SharePoint™ Portal Server, TAKE Solutions successfully demonstrated how PharmaReady achieves full management of SOPs, work instructions, and other documents regulated by the FDA easily and affordably. TAKE Solutions’ 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 |
| "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 |
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"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 TAKE’s solution." David Gardner, President |
InterDoc has been a leader in the Canadian pharmaceutical industry for many years. "TAKE’s 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 TAKE Solutions’ 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 |
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"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 |
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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 |
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"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 |
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“Some of the vendors we considered were large, well-respected companies – giants in the field. With TAKE Solutions’ PharmaReady DMS, two words come to mind – value and attentiveness. TAKE Solutions really listens to my input. I was pleasantly surprised when I purchased their new version of PharmaReady and saw that my suggestions had been implemented.” Pamela Haswell, Director of Regulatory Affairs |
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"The PharmaReady eCTD solution came at the perfect time for Banner Pharmacaps. Banner successfully utilized PharmaReady 4.1 for our recent eCTD submission to FDA. TAKE Solutions, Inc.’s knowledge and experience in both regulatory matters and information technology has made them an ideal business partner for us. Following our review of several industry solutions we concluded PharmaReady to be the most suitable eCTD solution on the market today to meet Banner's needs. Several key factors considered in selecting PharmaReady was their responsiveness to our questions and needs, ease of use of the tool and the fact that PharmaReady meets both FDA and EU regulations. Banner will use this tool for our Global regulatory needs where eCTD submissions are accepted. Any life sciences organization that’s under-going plans for an electronic submission should give the TAKE Solutions’ team and their PharmaReady™ eCTD solution careful consideration."
Dana Toops, Executive Director, Regulatory Affairs and R&D |
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In the highly regulated pharmaceutical industry, Alimera Sciences must carefully document its SOPs and training for all aspects of testing. "After networking with some colleagues in the Drug Information Association, we developed a list of about half a dozen candidate products and began researching each one. We zeroed in on PharmaReady DMS from PharmaReady, based on a combination of functionality and cost." Barbara Bauschka, Regulatory Affairs Associate Director |






