"TransPerfect clients have benefitted from Trial Interactive's versatile functionality, which includes solutions for eTMF, study start-up, and e-feasibility, as well as document management and learning management systems," said Michael Smyth, General Manager for TransPerfect Life Sciences. "In addition, Trial Interactive integrates directly with a leading Central IRB/Ethics Committee, further accelerating the site activation process for study teams. Now, this new release addresses the broadest possible set of needs around document management and quality systems."
Liz Elting, Co-CEO of TransPerfect, commented, "Our goal with Trial Interactive is to continually improve what we feel is the most versatile e-clinical technology on the market, and to improve transparency and streamline studies for our clients. This new release is a big step forward in allowing greater control, and in turn, enabling more effective and efficient study management."
Highlights of the new Trial Interactive:
- Refreshed user interface has a CTMS appearance and the flexibility to summarize system activity in dashboard visuals, which can be configured as needed by study.
- DocuSign provides 21 CFR Part 11 compliant e-signature capability for documents.
- Online editing features allow for annotations, version control, and other document review tasks.
- Integration with PleaseReview offers a robust tool for authoring, collaboration, version control, and template management to streamline document development and release.
- Learning management system (LMS) provides simplified training solutions for internal and external stakeholders with the ability to create custom e-learning modules that are more robust than just SOPs.
- Integration with eTMF allows certificates to be automatically routed to select folders to improve eTMF health.
"This newest release of Trial Interactive offers a better user experience in a versatile tool that offers so much functionality that clients can reduce the number of technologies upon which they rely," said Phil Shawe, Co-CEO of TransPerfect. "By improving team communications, enhancing security, and adding functionality in an already-familiar environment, we anticipate that clients both old and new will be thrilled with this new release."
About TransPerfect Trial Interactive
TransPerfect's Trial Interactive solution provides a collaborative web-based platform for study start-up and eTMF that enables sponsors, CROs, IRBs, central laboratories, and other vendors to maintain and update clinical trial documentation in a secure online environment. With fully searchable solutions including investigator portals, Trial Interactive streamlines study timelines and reduces the administrative burdens of global clinical trials. As part of TransPerfect's Life Sciences division, Trial Interactive is dedicated to working with clients on a global, collaborative level, supporting a wide range of requirements including e-feasibility, eTMF review/reconciliation, pharmacovigilance and safety management, endpoint adjudication, and product licensing and alliance management. For more information on Trial Interactive, please contact firstname.lastname@example.org or +1 212.400.8848, or visit www.trialinteractive.com.
With annual revenues of more than $500 million, TransPerfect is the world's largest privately held provider of language services and technology solutions. From offices in 90 cities on six continents, TransPerfect offers a full range of services in 170+ languages to clients worldwide. More than 3,000 global organizations employ TransPerfect's GlobalLink® Product Suite to simplify management of multilingual content. With an unparalleled commitment to quality and client service, TransPerfect is fully ISO 9001 and EN 15038 certified. TransPerfect has global headquarters in New York, with regional headquarters in London and Hong Kong. For more information, please visit our website at www.transperfect.com.
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