
TRANSPERFECT
For over 20 years, TransPerfect has helped life sciences companies conduct clinical development and commercialize products on a global scale. We bring that same level of expertise to our secure, web-based e-clinical solution, Trial Interactive.
Trial Interactive enables life sciences companies to streamline the execution and commercialization of global clinical trials and collaborate on partnerships while reducing administrative burdens. As a 21 CFR Part 11 solution, Trial Interactive also provides users with a completely secure environment in which to complete all required regulatory information, paving the way for paperless global clinical development and commercialization.
Our solutions are used by pharmaceutical, biotechnology, and medical device companies as well as CROs, IRBs/ECs and leading academic institutions involved in clinical development that stand up to the scrutiny of regulatory authorities globally. As near real-time access becomes even more critical to development and management teams around the world, Trial Interactive provides a hosted SOC 2 Type II certified environment with next-generation encryption and intrusion detection to protect your confidential information.
Contact TransPerfect today to find out how our solutions can streamline your development and commercialization activities.
FEATURED ARTICLES
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Speakers provide insight into how clinical teams can better manage their drug development studies and associated trial master files.
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Take a deep dive into the pivotal enhancements within the GCP E6(R3) ICH Harmonized Guidelines that are expected to have a substantial influence on trial execution and documentation.
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Feel confident that your study team training practices are comprehensive and aligned with both regulatory and corporate mandates by watching this presentation by Trial Interactive's Product Manager, GlobalLearn, Marc Gracieux.
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Utilize this comprehensive checklist as a guiding framework to formulate a robust high-level plan that encompasses CTMS requisites and outlines the necessary training and documentation.
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Watch as TransPerfect Life Sciences Executive Director Pierre-Frederic Omnes explores topics surrounding trial transitions and answers common questions regarding new European requirements.
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Gain insight from Trial Interactive’s Director of Client Solutions Laurel-Ann Schrader who outlines the top five skills team members should prioritize for their professional development.
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Gain invaluable wisdom that can be applied to life sciences dealmaking from AstraZeneca and Merck's remarkable panel of experts.
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Consider these 10 questions when interacting with ChatGPT about how to improve patient recruitment, engagement, and retention efforts in your next clinical trial.
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Gain valuable insights and enhance the efficiency of app localization processes to ensure a smooth and multilingual patient experience, while also complying with local regulations and privacy laws.
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Learn how automation can help fulfill new MDR/IVDR requirements and optimize existing labeling and documentation operations while meeting compliance.
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Gain a comprehensive understanding of the Clinical Trial Regulation (EU) 536/2014 (CTR), which has equipped stakeholders to navigate the altered regulatory landscape and prepare for conducting clinical trials in the EU/EEA.
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Learn how by looking at the advantages of wearables and where they are headed in the future, manufacturers, providers, and researchers can better anticipate collaboration efforts to bridge the gaps in existing processes and maximize the potential of eCOA wearables in clinical research.
CONTACT INFORMATION
TransPerfect
3 Park Ave
New York, NY 10016
UNITED STATES
Phone: 877.523.4888
PRODUCTS
PRESS RELEASES
- Expediting Site Activation With TI Study Start-Up
- The TI Platform In One Unified App
- TI Clinical Content Collaboration: Simplify Clinical Document Lifecycles
- Quality Management Solutions
- Trial Interactive Quality Management Solutions
- Centralize Your Labeling Workflow Management
- Trial Interactive’s Transport Integration
- Create Easily Understandable Summaries Of Results For Every Trial
- Connect During Your Patient’s Journey
- COA & eCOA Solutions