Global Lunch and Learn for Clinical Operations – SterlingBio Smart CRO Services and Solutions

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Global Lunch and Learn Series For Clinical Operations

clinical trials event description

Are clinical trial startup processes taking too much time?   Research shows that clinical site initiation times can take 7 months or longer on average.     This global lunch and learn series for clinical operations will explore best practices and real world examples of how companies like Clinilabs Drug Development Corporation are streamlining clinical trial startup processes and in some cases, cutting startup time in half using tools such as eClinical applications automation, investigator portals and FDA Part 11 Adobe Digital Certificate Signing.

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SureClinical

The We Care CRO

Customers and Users

"Our users, sponsors, and investigators are delighted by SterlingBio's SureClinical suite of eClinical applications, including SureCTMS, SureETMF, and SureDrive."
Gary ZammitCEO of Clinilabs Drug Development Corporation
Gary Zammit
"Of all of the systems I use, SterlingBio's SureClinical apps and platform are the best for Clinical Trial Management."
Deana DowdCRA Consultant, First Coast Clinical Research
“With SterlingBio's SureClinical apps and platform, we cut our clinical trial project startup time in half. Going digital was not only a significant time saver, but it also enhanced the quality of our data.”
Global CRO
Global CRO
"With SterlingBio's SureETMF, internal and external study stakeholders can collaboratively complete, digitally sign and share regulatory and study information in the cloud from mobile or web. This strategic capability allows us to eliminate paper at point of origin, accelerating document completion and enhancing document quality."
Lynda ShelleyClinical Operations Exec Director
”With SterlingBio's SureClinical apps and platform, our goals of going digital have been met. We tested and sandboxed many systems before making the decision to go with SureClinical for SureETMF and SureCTMS. Our own client users are passionate about the software and it is incredibly easy to initiate, file and manage documents and trials."
Global CRO
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