Thought Leadership
How to Approach the Protection of Personal Data and Commercially Confidential Information of EU Clinical Trial Applications: Practical Considerations
In this piece, we'll explore the two primary frameworks that are driving EU CTR transparency efforts: the European Medicines Agency’s Policy 70 and Regulation (EU) No. 536/2014 on clinical trials. Gain valuable insight into requirements, exceptions, and implications for all...
Localizing Platforms for Digital Health: The Importance of Post-Localization Context Review
In a landscape defined by continuous technological advancement, many organizations in the life sciences industry strive to increase audience engagement through digital modalities, such as mobile and web applications or web portals. Building a robust technological...
Achieving Global Success in Clinical Trial Recruitment
TransPerfect's GlobalLink Connect integration with Adobe Experience Cloud enabled one of the world’s largest pharmaceutical companies to help visitors in 17 countries and 13 languages identify clinical trials that might be right for them or their loved ones....
Medical Writing Services Increase Patient Comprehension
“The informed consent form and companion piece were super! Overall, the feed back we received from our patient advocacy panel was great and they found the content useful, clear, and relevant.”...
3 Translation Methodologies for Life Sciences Documentation
This post outlines three translation methodologies for life sciences documentation, emphasizing their importance due to the complexity and specific needs of clinical documentation translation. It describes standard translation, back translation & reconciliation, and...
How to Increase Your Likelihood of Scientific Publication
Writing a scientific manuscript involves considerable planning and organization to boost your chances of publication in a peer-reviewed journal. Here, we show you how to develop a thorough plan to present research logically and how to avoid the common pitfalls of authorship, so...