Pharma Services Category of TransPerfect

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We enable global clinical development teams to rapidly translate and share pharmacovigilance information, such as SUSARs (suspected unexpected serious adverse reactions), SAEs (serious adverse events), hospitalization reports, and discharge summaries, within a centralized collaborative workspace.

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With more than 300 drug products and vaccines currently in clinical trials, TransPerfect's expertise in medical and life science translation and language services provides the quality, efficiency, and reliability necessary to compete in this fast-paced industry.

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Consecutive & escort interpretation, simultaneous/conference interpretation, remote/over-the-phone interpretation

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TransPerfect is proud to offer Trial Interactive, our 21 CFR Part 11 compliant, web-based e-clinical solution

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Trial Interactive is the all-inclusive source for all of your clinical data management needs. In addition to hosting clinical trial solutions and electronic case site solutions, we also provide a full array of scanning and clinical document management services.

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TransPerfect's multilingual e-clinical solution creates a scalable solution to securely manage Clinical Outcome Assessments and all related documentation, significantly increasing efficiencies in the clinical development and trial processes while giving secure visibility to all internal and

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TransPerfect has developed Trial Interactive–the world's only clinical trial solution specifically designed to meet the needs of life sciences. Now, companies that are participating in licensing activities can securely share confidential product development information through an easy-to-use,

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TransPerfect’s eFeasibility solution allows investigators to populate information into a web survey, then relaying the information to the investigators. These surveys can be done completely online or they can be printed out and done in hard copy, and uploaded via email or fax upon preference.

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The Trial Interactive eISF offers a complete solution for electronic distribution, collection and management of essential investigator site files.

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Trial Interactive includes workflow to promptly facilitate the review and approval by the trial sponsor and then provides an organized, searchable electronic Regulatory Binder as well as Study Binders if required by the sponsor or institution.

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Trial Interactive provides companies with the ability to set up eTMFs in a matter of hours and can even be organized based on the file structure which is currently in place, allowing access to internal users as well as any partners with high level security access.

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Trial Interactive provides a collaborative work space for all relevant stakeholders – including investigative site personnel, core labs, and study teams – where these cases can be collected and delivered to adjudicators.

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TransPerfect's device-independent call center solutions allow you to easily and affordably route calls to our global call centers where we intake and process cases, either as part of a clinical trial or in supporting post-marketing pharmacovigilance efforts

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TransPerfect LMS can help you assist with meeting your global regulatory training requirements.

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eCTD preparation and review, global CTA submissions, Packaging and labeling translation