Quality Solutions That Reduce Compliance Risks in Clinical Trials

Choose from specialized solutions that help you increase quality and efficiency. 

Get in Touch
Person on computer running quality assurance check

Why QA Teams Love TransPerfect

Our knowledge and experience in Quality Management is evidenced by our ability to create and curate strategic solutions to improve day-to-day operations / reducing administrative burdens. We have 30+ years of experience customizing these solutions. Here are some of your options:

    QMS Powered by Trial Interactive

    Our suite of eClinical solutions—part of TransPerfect’s Trial Interactive™ offering—improves visibility, reduces timelines, enhances quality, and mitigates risk. Explore our solutions for quality management, training management, audit management, vendor oversight, quality documents, and more.

    Learn More

    Training and Development

    We offer training support across any platform, in 200+ languages, and any subject matter. Our team centralizes your global learning requirements and manages the administrative work, so you can roll out your content quickly and cost-effectively.

    Learn More

    Language/Translation Solutions

    Ensure conceptual equivalence and cultural appropriateness in any language, minimizing time-to-market, mitigating risk, and ensuring compliance in global studies.

    Learn More

    Your Partner in Risk Mitigation

    Ensuring quality from R&D through commercialization is complex due to ever-evolving regulations, international policy, and corporate change, among many other variables. QA teams need all the support they can get to embed quality in the organizational culture through efficiencies such as digital and automated work streams, real-time oversight, e-learning, and translated quality documentation for multilingual operations.

    Improved Outcomes by the Numbers

    85% of clinical trials experience delays. Mitigating compliance risks by streamlining QA operations is a key strategy for preventing costly delays caused by CAPAs and inspection findings.

    1.2 M

    Saved by CRAs using our CTMS for day-to-day operations


    7.5 k

    Studies managed in Trial Interactive

    100 +

    TMFs rescued mid-study

    3 k

    eTMF study migrations completed

    50 %

    Faster site activation

    News and Thought Leadership

    Industry insights from our experts. We have the experience and solutions you need to navigate life sciences complexity and bring breakthroughs from lab to launch.

    Your Multilingual Trial Site SEO Success Checklist

    Multilingual trial SEO is critical to ensure that patients and HCPs can actually find and act on your trial content in their language. This checklist walks clinical trial teams through five essentials:… ...

    Your Multilingual Trial Site SEO Success Checklist

    Clinical Trials Translation Management: A Scalable Workflow for Faster Enrollment

    When it comes to clinical trials, website localization isn’t just about translating words into other languages. It’s about designing a governed, repeatable workflow that keeps every multilingual page accurate, reviewable, and in sync as content changes. This ensures patients,...

    7 Workflow Hacks for Smarter Clinical Trial Localization

    Imagine this: a director of clinical operations at a mid-size pharma needs better regional recruitment to hit aggressive enrollment deadlines. So, they push to launch the company website in nine languages at once. The moment the request lands, the clinical compliance manager...

    LifeSci Talks COA Series | Building Fit-for-Purpose PRO Instruments: Focused Modern Measures Over General Instruments

    In this episode of LifeSci Talks, Mark Wade, Global Practice Leader & COA SME at TransPerfect Life Sciences, is joined by Katja Rudell, VP of Patient-Centered Outcomes at Kielo Research, to take a behind-the-scenes look at the reality of patient-centered instrument ...

    How Medical Communications Teams Can Scale Reviews Without Sacrificing Speed

    Medical communications teams are under mounting pressure to review more content than ever before without adding headcount or increasing risk. This white paper outlines five pillars for rethinking MLR workflows, from modular content and tiered reviews to automation and governance. ...

    Patient Recruitment: Clinical Research's Costliest Bottleneck

    Patient recruitment is the costliest bottleneck in clinical research. Learn proven strategies to reduce study delays, optimize enrollment, and cut regrettable spend. ...

    From Draft to Deployment: Creating Global-Ready Content from the Start

    Clinical, regulatory, and commercial teams all rely on the same content, yet often work in siloes. This white paper examines the real cost of disconnected content strategies and why localization should be treated as a strategic input, not a final step. Discover how global-ready ...

    Trusted by Life Sciences Organizations Big and Small

    Gilead
    Boehringer Ingelheim
    Syneos Health
    Vertex
    Bayer
    Johnson & Johnson logo
    IQVIA
    CVS Health
    BMS
    Merck
    Biogen
    Novartis
    Pfizer logo
    Roche logo

    Working in QA? Let’s connect.