Thought Leadership

7 Essential Steps to Reach Global Audiences with Website Localization Services for Life Sciences Organizations

Website Localization for Life Sciences Organizations Means Greater Global Reach Life sciences organizations are under increasing pressure to connect with global audiences. With 65% of internet users preferring websites in their native language and 40% refusing to buy from...

PPT Resource: Harnessing AI in Pharmacovigilance: Insights from World Drug Safety Amsterdam 2024

Pharmacovigilance professionals face an escalating challenge: data overload. From AI-powered transcription and case triage to automated literature translation, insights from the World Drug Safety Congress 2024 showcased practical solutions for streamlining workflows and reducing...

Harnessing AI in Pharmacovigilance: Insights from World Drug Safety Amsterdam 2024

Introduction In the pharmacovigilance space, the overwhelming trend in the current landscape is data overload. Increasingly unmanageable volumes of information pose a core challenge for today’s pharmacovigilance professionals. While digital transformation and new technologies...

LifeSci Talks | Effective Rater Training: A Critical but Overlooked Part of COA Administration

In this episode of LifeSci Talks, TransPerfect Life Sciences’ Global Practice Leader Mark Wade sits down with Kelly Dumais PhD, Director of eCOA Science at Clario to discuss the significance rater training plays in standardizing the administration and scoring of clinical scales....

The Mindset Shift: Integrating Digital Strategies to Enhance Medical Affairs

In today’s evolving healthcare landscape, the role of medical affairs has been undergoing a transformation from a supportive function to a key strategic player. This shift is prompting medical teams to explore digital innovations and offer efficiencies with scaled practices. ...

Xtalks Webinar: Artificial Intelligence and Structured Data: Driving Process Efficiency for Medical Device Manufacturers

As more and more clinical trials are conducted internationally, with a higher level of protocol complexity, and with increased competition to get medical products to market faster globally, the need for efficient and streamlined clinical product development is greater than ever. ...

AI and MT for Regulatory and Clinical Content Office Hours - 10/9/24

TransPerfect's experts gather to answer questions from global pharma, biotech, and medical device leaders regarding AI and MT use cases, challenges, opportunities, best practices, and more....

Scaling Global Campaigns with AI and Human Expertise: Lessons from Sanofi

Navigating the complexities of global healthcare campaigns requires a well-balanced mix of technology and human touch. In this webinar, TransPerfect welcomes back Krista Goedel, Clinical Digital Content Lead along with colleague Lyly Fong, Global Corporate Website Manager at...

LifeSci Talks COA Series | From Interview to Endpoint: Understanding the Importance of Patient Listening to Build Better Outcomes

In this episode of TransPerfect LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences sits down with John Reites, Co-Founder and CEO of THREAD research to discuss the importance of patient listening to build better clinical trial endpoints. They delve...

Accelerating Clinical Product Development through Centralized Content Work Streams

As more and more clinical trials are conducted internationally, with a higher level of protocol complexity, and with increased competition to get medical products to market faster globally, the need for efficient and streamlined clinical product development is greater than ever. ...

Transcreation in Clinical Research: How to Use Transcreation and Localization to Resonate with Your Audience

Clinical teams need to communicate with multilingual audiences across the globe while also meeting strict regulatory requirements. In addition to helping teams remain compliant, accurate translations ensure the highest standards of patient safety are met across clinical...

Where to Apply Machine Translation in Life Sciences Content Workstreams Right Now

In the life sciences industry, it’s increasingly essential to reduce cycle times and enhance operational efficiencies, especially across clinical and commercial team processes. To address evolving regulations from global health authorities and the common pain points of costs,...

The Imperative of Accurate Translations in Clinical Research

With the increase of global clinical trials, clinical documentation is required to be accurately translated at every stage from lab to launch. Despite the administrative burdens and tight regulatory timelines that clinical teams face, accuracy cannot be sacrificed in life science...

How Pharmacovigilance Automation Solutions Can Help You Meet Tight Regulatory Reporting Timelines

Pharmacovigilance (PV) teams play a critical role in detecting, assessing, understanding, and preventing the unintended adverse effects of medications and treatments. Their work, which includes drug reaction monitoring, drug safety surveillance, side effect monitoring,...

How to Improve the Speed and Accuracy of Patient Communications in Clinical Development

According to Phesi, more than a quarter of clinical trials conducted in 2023 were canceled during Phase II.  As clinical research teams struggle with patient recruitment and engagement under tight deadlines and immense regulatory pressure, patients also grapple with...

Implications of AI in Healthcare and Life Sciences: Ethical Considerations in the Age of AI

Artificial intelligence (AI) models have already shown transformative potential in the life sciences industry, including automating administrative clinical research tasks, analyzing patient data to predict future health risks, synthesizing medical information, and more. ...

The Ultimate Guide to AI in Pharmacovigilance and Safety Reporting

Pharmaceutical companies face stringent compliance requirements and tight deadlines for reporting safety cases throughout clinical research and development. To protect patient safety and avoid penalties from regulatory authorities, pharmacovigilance teams must submit in-language...

E-Learning in Pharma: Creating & Managing Global Training Programs

From compliance and standard operating procedures (SOPs), to product info and sales techniques, e-learning ensures global teams have access to top-notch, consistent, and on-demand training. This guide explores key considerations for effective and engaging global e-learning...

Pragmatic Use Cases for AI in Pharmacovigilance and Safety

The rapid rise of artificial intelligence presents an opportunity for effective and transformative applications in pharmacovigilance. Intake, query routing and response, case reporting, HAQs, and more are now extremely feasible use cases that create exponential efficiency in...

3 Ways to Leverage Generative AI in Pharmacovigilance

Despite the rigorous drug safety and efficacy standards in trials, study medicines can have unintended side effects on patients throughout the clinical trial journey and even in the post-market setting. To ensure patient safety and mitigate risk, global health regulatory...

Human & Animal Blood Cell Image Annotation Spotlight

An award-winning healthcare AI company specializing in using the best in human and computational intelligence approached DataForce to build an external team with a background in biology to review and annotate thousands of microscopic images of blood smear samples. With 30,000...

How to Select the Right Regulatory Writing Company for Your Organization's Needs

In a landscape defined by ever-evolving global guidelines from health authorities, many life sciences organizations’ clinical and regulatory teams face challenges in navigating the regulatory affairs writing and document submission process. Adhering to strict rules while...

5 Essential Use Cases for Generative AI and Machine Translation in Regulatory Content Submissions

Moving a drug from development, through clinical trials, to eventually the market involves many critical content pieces and challenges along the way.   According to research commissioned by Genpact, 72% of senior executives across the life sciences industry cited regulatory...

eCOA Vendor Localization Best Practices Checklist

One of the main challenges for pharma/biotech companies regarding clinical trials is prolonged eCOA study start-up. It is paramount to choose the right eCOA platform for each study. Sponsors must consider the study’s specific needs, such as user-friendliness, compliance, and...