Quality Solutions That Reduce Compliance Risks in Clinical Trials
Choose from specialized solutions that help you increase quality and efficiency.Learn More
Specialized Services and Technology to Support Global Clinical Trial Operations
From e-learning and training management to quality document management technology and language services, our comprehensive solutions are designed to meet the QA needs of life sciences companies. Our experience, expertise, and technology support global product development by helping to ensure corporate and regulatory compliance.
Training Management and Course Development
Launch effective training and reduce training expenses. Get support with authoring training content, videos, and eLearning for compliance and streamline training delivery with LMS technology designed for global study teams and clinical sites. With Training Management, send approved and effective policy and SOPs directly to the LMS for "Read & Understand" or eSignature by staff to ensure training compliance.Learn More
Ensure the accuracy and consistency of global training content and simplify the rollout of multilingual training programs with industry-leading translation automation and service solutions for localization, adaptation, managed in-country review, and more. Ensure compliance with seamless "Author-to-Archive" workflows between your content repository and certified translation staff with TransPort to TI connectors.Learn More
QMS and Quality Documentation (Trial Interactive)
Simplify quality management with a centralized workspace where you can create quality document templates; track them through draft, review, and approval; and then seamlessly publish to the LMS as learning modules to enforce compliance. Track and manage complaints, investigations, CAPA, audits, observations and findings, actions, effectiveness checks, and change management using standard best-practice QA workflows for GCP and GMP.Learn More
Achieve Greatness in the Global Regulatory Landscape
Today, global sponsors are consistently challenged to bring products to market faster while facing evolving regulations with increased scrutiny. With the language barriers and collaboration logistics of global operations, clinical trials must be managed carefully to avoid unexpected increases in cost, time, and compliance risk. Having a global partner like TransPerfect by your side helps you focus on what matters most: saving lives.
Improved Outcomes by the Numbers
Saved by CRAs using our CTMS for day-to-day operations
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.
Studies actively managed in Trial Interactive
TMFs rescued mid study
eTMF study migrations completed
Faster site activation
Trusted by Life Sciences Organizations Big and Small
Join TransPerfect's community of more than 1,000 life sciences organizations, including pharma and biotech, CROs, IRBs, and agencies.