
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.
CONTACT INFORMATION
TransPerfect
3 Park Ave
New York, NY 10016
UNITED STATES
Phone: 877.523.4888
PRODUCTS
- Trial Interactive 10.2
- Central Laboratory Solutions
- Study Start Up
- Clinical Development Document Management
- Pharmacovigilance System Master File
- Electronic Regulatory & Study Binders
- Global Clinical Trial Support
- Institutional Review Board (IRB) Solutions
- Cinical Trial Interactive Solution: Due Diligence
- Global Multilingual Call Center
- Electronic Trial Master Files
- Endpoint Adjudication
FEATURED ARTICLES
- Practical Applications For Machine Learning In Clinical Trials
- 4 Machine Learning Use Cases for Clinical Trials
- Driving Fundamentals: Ensuring An Efficient Clinical Research Process Trial Management
- What Is A TMF Certified Copy?
- The Paper Chase: Clinical Outcomes Assessments In The Digital Age
- Best Practices For Preparing For Your TMF Inspection
- How To Improve Medical Literature Review With Technology
- From Industry Recommendations To Reality – What’s New In The TMF Reference Model 3.2.0
- Say “Yes!” To Mobile-First CTMS
- Remote Trial Management: Remote Investigator Meetings And Site Initiation Visits
- Swimming In A Data Lake Of eCOA Wearables
- Back To The Basics Part 1: What Is An eTMF?
- 4 Ways To Avoid COA Source Revisions And Mitigate Risk In Your Global Clinical Trials
- Navigating The CMS Requirements For Medicare Advantage Plans In The Wake Of COVID-19
- Establishing A Culture Of Inspection Readiness
- Getting Started With Remote Trial Management
- Plain-Language Abstracts: A Benefit To Your Research
- Best Practice For Using Technology And AI To Manage The End-to-End Medical Information Content Lifecycle
- Globalization Of Clinical Trial Registration In Light Of COVID-19
- Prospective Writing To Prepare Disclosure-Ready Clinical Trial Documentation
- 5 Key Considerations When Moving To Remote Monitoring In Our Ongoing Clinical Trials
- A Summary Of FDA Guidance On COVID-19: Patient Safety And Adapting Processes
- Clinical Delivery Within COVID-19: We Have The Ability To Adapt
- Machine Learning In The eTMF: Human-Aided Active Learning Processes
- Kicking It With DPharm
- An Overview Of TMF Oversight—Part 1: Keeping An Eye On Your Vendors
- Lay Summary Development—The Oregon Trail Of Regulatory Writing
- When It Comes To Your Patient Adherence (Compliance) Strategy, Think Training
- The Science And Art Of Design Thinking
- Evolving With Our Clinical Users – Part 2
- Evolving With Our Clinical Users – Part 1
- First Thoughts After ISOQOL 2018
- China’s Recent Drug Scandals: What Do They Mean For Foreign Drug Makers?
- TMF Summits In Europe And OCT Barcelona: Talking About The Future Of TMF
- DIA Session Recap: Automated Translations For Pharma Companies
- 10 Things We’ve Learned In 10 Years Of E-Clinical Innovation: Part 3
- 10 Things We’ve Learned In 10 Years Of E-Clinical Innovation: Part 2
- 10 Things We’ve Learned In 10 Years Of E-Clinical Innovation: Part 1
- GDPR: New Considerations And Shared Experiences For Life Sciences Companies
- Challenges, Change, And The Future Of eTMF
- eTMF + IRB Integration = Efficiency
- Paperless Clinical Trials: How And Why
- Here’s To Your eTMF Health
- How To Streamline Your Global Pharmacovigilance Management Process
- ETMF And Site Archiving: Perspective, Case Studies, Lessons Learned
- A “Holistic” e-Clinical System: Be Wary of Managing Clinical Development With Blinders On
- Global Call Centers For Life Sciences Organizations
- Moving Towards An Electronic Environment In Clinical Trials
- New Molecular Entities (NMEs) - The Path Of Resistance
- 4 Ways You Can Overcome Roadblocks To Technology Adoption In Clinical Trials
- Resourceful Resourcing: Consolidate Your Technology Providers
- Assessing Efficacy Of Our Life Saving Drugs
PRESS RELEASES
- Transperfect Life Sciences Announces Free Access To Trial Interactive Central And Remote Monitoring Solutions For Study Teams Impacted By COVID-19
- TransPerfect Life Sciences Takes Center Stage At DIA 2019 With A Theatrical Stakeholder Collaboration Workshop
- TransPerfect Life Sciences Expands Leadership Team With Senior E-Clinical Industry Expert Hires
- Agility Clinical Chooses TransPerfect As ETMF Provider
- Regado Biosciences Selects TransPerfect’s Trial Interactive Platform As Its Study Start-Up And eTMF Solution
- Aptalis Selects Transperfect’s Trial Interactive Technology As Its Pharmacovigilance System Master File (Psmf) Solution
- Biocom Selects TransPerfect For E-Clinical Technology And Translation Services