Thought Leadership
Enabling Diversity & Inclusion in Clinical Trials: A CRO & IRB Perspective
Diversity in clinical research is imperative to ensure the safety and effectiveness of drugs and medical devices for all people—and everyone in the industry is a key stakeholder. Clinical trials today still lack ethnic diversity, and to make trials more inclusive and improve...
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...
UMotif - Empowering Patients to Drive Engagement and Adherence
Watch this presentation on how empowering patients with cloud solutions increases engagement. ...
TransPerfect’s GlobalLink Helps Top-10 Pharma Meet their EC Deadlines in More than 20 Countries
A top 10 pharma company was facing delays in EC submission deadlines for their global studies....
Lessons Learned in the Rush for a Vaccine and the Effects on Language Translation: Creating and Adapting Technologies
The rush to a vaccine has accelerated an already dynamic research process. This has led to many innovations and an evolution of procedures. The language translation industry has seen enormous stressors and has had to create and modify processes and technologies similarly. The...
ISPOR Europe 2020 Virtual Poster - Usability Testing for eCOAs
In order to ensure a fluid experience for a patient, usability testing is a critical data point to consider. Addressing both a patient’s needs and access to a digital platform is key to data collection. TransPerfect, along with our partners from Parexel, Clinical Ink, and...
Medical Annotation: Using Natural Language Processing for Adverse Events
TransPerfect's DataForce Streamlines Adverse Event Detection with NLP. ...
The Paper Chase - Clinical Outcome Assessments in the Digital Age
Patients are, at last, gaining a voice in healthcare. Stakeholders have come to recognize that patients have valuable information to share about their experiences with diseases and medications that should influence policy and treatment decisions. The U.S. Food & Drug...
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...
Artificial Intelligence in Life Sciences: Latest Developments Presented by Industry Leaders
Join TransPerfect's discussion with industry-experts from Pfizer, Bayer, CodaMetrix, Biogen, BI, Novartis, and Syneos Health about how AI is accelerating changes in the life sciences industry and ways they are leveraging data to support their teams, studies, and products. ...
Swimming in a Data Lake of eCOA Wearables
We all know there is a significant increase in data collected from wearable sensors, but what does that mean for eCOA? In our latest whitepaper , Mark Wade, Global Practice Leader for TransPerfect Life Sciences examines the considerations of adopting these sensors as an addition...
Part 4: Clinical Trials and COVID-19: Remote Investigator Meetings
The novel COVID-19 virus has forced a lot of rapid changes in a very short period. Personally and professionally, we are all learning how to adapt. While restrictions on our day-to-day lives impact where, why, and how we interact, we still can come together as a community to...
Driving Strategic Change: General Counsel in Pharma
TransPerfect Legal Solutions hosted a panel of GCs and legal experts from prominent pharmaceutical companies to discuss their evolving roles and the practical ways legal departments are driving innovation as it relates to people, risk, and data in the pharma industry. ...
TrialScope - NOT Lost in Translation - Multiple Languages Key for Trial Websites
OneLink helps Bayer launch clinical trial websites faster and cost-efficiently. ...
Part 3: Clinical Trials and COVID-19 Adapting to Rapid Change
The novel COVID-19 virus has forced a lot of rapid change in a very short period of time. Personally and professionally, we are all learning how to adapt. While restrictions on our day-today lives impact where, why, and how we interact, we still can come together as a community...
Part 2: Clinical Trials and COVID-19 Converting to Remote Trial Management – How to Get Started
The novel COVID-19 virus has forced a lot of rapid changes in a very short period. Personally and professionally, we are all learning how to adapt. While restrictions on our day-to-day lives impact where, why, and how we interact, we still can come together as a community to...
Simplifying Clinical Trial Training Management
Training is important and required to remain current with appropiate regulations. This is key to protecting patient safety and putting out quality products....
Trial Interactive Speeds FDA Approval for Myeloma Patients
TransPerfect's Trial Interactive eTMF, TMF services, and translation services enable Karyopharm to expedite FDA approval. ...
TransPerfect's OneLink Enables BI to Focus on Saving 1000 Lives
The case study highlights how TransPerfect Life Sciences helped Angelini Pharma overcome language barriers in clinical trials, enabling efficient communication and regulatory compliance....