Thought Leadership
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...
Automation for MDR & IVDR: A Three-Part Seminar - Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements
Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements...
Automation for MDR & IVDR: A Three-Part Seminar - Part 2: Structured Content and CCMS Technology to meet MDR & IVDR requirements: Takeda Medical Device Group, Qserve, & TransPerfect Medical Device Solutions
Part 2: What is a CCMS and How Does It Address the Challenges Posed by MDR and IVDR?...
Automation for MDR and IVDR: A Three-Part Seminar - Part 1: What Is a CCMS and How Does It Address the Challenges Posed by MDR and IVDR?
Part 1: What is a CCMS and How Does It Address the Challenges Posed by MDR and IVDR?...
Panel: Deploying AI for Translation - Real Life Examples
Learn how leading companies deploy machine translation and the results they are seeing from their MT strategy. ...
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. ...
Pfizer - Unlocking the Power of GlobalLink Within Pfizer Medical Information
GlobalLink and AI enable faster, better decisions in response to patient queries. ...
Rapidly Bringing HCP Support Tools to Global Markets at Scale
GlobalLinks helps AstraZeneca launch HCP tools around the world. ...