Thought Leadership
Multilingual Labeling: Considerations for Efficient, Cost Effective and Compliance Labeling
Accurate and compliant labeling of an investigational medicinal product (IMP) is an important and integral part of clinical trial operations. A misstep in labeling can lead to significant delays, affecting the entire study’s timeline and potentially incurring costs ranging from ...
Unlocking the Power of AI and Machine Learning in Life Sciences
Life sciences companies are putting artificial intelligence (AI) and machine learning (ML) into practice, realizing its potential to revolutionize adverse event detection, diagnostics, and more. For AI and ML to be truly effective, you need to give context to your data, teaching...
Navigating the EU Clinical Trial Regulation Complexities - Current Challenges and Opportunities
As the most significant change in the European Union clinical trial legislative ecosystem in 20 years, the European Union Clinical Trial Regulation 536/2014 (EU CTR) went live on January 31, 2022. The first-year transition period has now ended, and from January 31, 2023, EU...
Driving Digital Excellence: Delivering Seamless and Personalized Customer-Centric Experiences
The digital evolution in reaching and engaging with global communities, including sponsors, CROs, patients, and HCPs, has drastically shifted the way medical affairs teams connect with key stakeholders. As the industry pursues ways to improve a consumer and patient-centric...
Clinical Data Services Company Launches its Statistical Webinar Series
“Another great seminar in a long line of excellence. I can only say, keep it up!”...
Global Pharma Saves $1.1M with Regulatory Translation Solution
AI-powered workflows to help reduce costs and timelines while being scalable to the large volume of content required....
Content Automation to Meet MDR & IVDR Requirements
Marc Miller, President of TransPerfect's Medical Device Solutions chatted with experts from Takeda Pharmaceuticals & QServe to learn about MDR & IVDR labeling compliance while cutting risk, cost, & turnaround by using structured content, process automation, &...
Novo Nordisk Delivers Multilingual Digital Experiences Through GlobalLink and Adobe
"Before GlobalLink for AEM we had to manage translation processes outside AEM, adding an extra layer of processes and approval flows into our work stream. Now it all happens within the same system, making translation and approvals flows smoother."...
Sanofi - The Clinical Translation Centralization Journey in Light of the EUCTR 536/2014
Sanofi centralizes clinical trial translations through GlobalLink and best-in-class AI, MT, and more. ...
Rapidly Bringing HCP Support Tools to Global Markets at Scale
GlobalLinks helps AstraZeneca launch HCP tools around the world. ...
TransPerfect Supports Takeda Supply Chain Training with Gamification
“TransPerfect supported us on building a great learning experience for our community. Elements of gaming like point scoring and competition with others are incorporated in a training to learn our KPI definitions and targets.”...
UBC Case Study: UBC Expedites Administration and Contact Center Response Times
TransPerfect Connect helps UBC expedite administration and call center response times....
Interpreters Support Novartis Patient Engagement Team
TransPerfect interpreters and translation services support patient interviews to increase awareness of IRDs. ...
Content Solutions for MDR & IVDR Readiness
The implementation dates for MDR (May, 2021) and IVDR (May, 2022) are fast approaching and non-compliant manufacturers are putting their EU market access at risk. These new regulatory requirements have created a “tsunami” of increased content requirements—especially in critical...