Quality Solutions That Reduce Compliance Risks in Clinical Trials

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

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.

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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.

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Language/Translation Solutions

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

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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.

When Licensing Becomes the Bottleneck: Lessons from a Sponsor on COAs, eCOA Vendors, and Getting It Right

Blog

Clinical outcome assessment (COA) licensing has a reputation in the industry, and it's not a flattering one. "It is often called the bottleneck of COA," says Mark Wade, Global Practice Leader and COA SME, in a recent LifeSci Talks episode with Stacey Higgins, who holds nearly two decades of experience navigating licensing, vendor relationships, and global study complexity. What was discussed was not frustration, but rather a clear pattern of where sponsors tend to ...

When Licensing Becomes the Bottleneck: Lessons from a Sponsor on COAs, eCOA Vendors, and Getting It Right

Checklist

Audit-Ready Website Localization: A Checklist for Global Clinical Trials

Multilingual clinical trial websites often involve more than most teams anticipate and gaps rarely surface until an audit, a failed form submission, or a compliance review. The difference between a localized site that holds up under scrutiny and one that doesn't comes down ...

Guide

Website Localization Fact Sheet

Language barriers are a measurable enrollment risk, and one that compounds fast. With 25.7 million people in the US living with limited English proficiency and 41% of adults reporting they know nothing about clinical trials, the patient pool is larger than most teams realize and ...

Guide

Patient Recruitment Strategies for Clinical Trials

Most trials miss enrollment targets because patients don’t understand, trust, or act on the information they receive. The gap between a recruitment strategy built around patient comprehension and one that isn't, touches everything from screening drop-off to diversity goals. ...

Guide

Clinical Trial Website Localization: Accelerating Enrollment and Reducing Compliance Risk

Language barriers are a measurable enrollment risk, and one that compounds fast. The gap between a localized and non-localized clinical trial website is wider than most teams expect, touching everything from regulatory compliance to participant drop-off. This infographic breaks ...

Blog

Medical Device Localization: Navigating Compliance and Empowering Engagement

As medtech digital health ecosystems expand, companies face growing pressure to deliver products and information tailored to each global market. Meeting that demand requires a strategic approach to medical device translation and localization spanning cultural adaptation,...

Success Stories

Scaling Clinical and Regulatory Content with GlobalLink's Intelligent Performance

A Top 10 pharma needed to accelerate clinical and regulatory translations without increasing compliance risk or slowing submissions. This case study shows how they kept content inside Veeva Vault with an automated integration and a hybrid model (AI + validated translation memory ...