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 approach, an omnichannel medical strategy is critical for continuing to drive collaboration, improve customer relations and patient trust, and disseminate and distribute medical information to global audiences.
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, & advanced AI technology.
Shaping The Future of eCOA/ePRO
We have witnessed a rapid and dramatic migration from paper to electronic COA/PRO in the past few years. TransPerfect Life Sciences' C3 Summit brings to you virtual sessions on how the paper to digital migration is evolving, the use and application of eCOA migration technology, and setting up successful eCOA solutions.
Be Where Your Patients Are – Effective Digital Strategies For Patient Recruitment
Tuesday, August 24 | 11:00 – 11:30 AM

In this webinar, TPTDigital’s Director, Brian Hansen, will discuss how

  • Digital marketing is an easy, inexpensive, and effective tool for patient recruitment
  • TPTDigital helped Amarex, a global CRO, recruit LGBTQ, HIV positive patients for their study
  • CRO's can utilize digital best practices to ensure successful patient recruitment
Diversity & Inclusion in Clinical Trials: A CRO & IRB Perspective
Tuesday, June 22 | 11:00 AM EST
In this webinar, Amanda Ryan, President of G3 Life Sciences, will speak with Aman Khera, VP of Global Regulatory Strategy at Worldwide Clinical Trials, and Luke Gelinas, Advarra’s IRB Chair and Senior Advisor, about their perspective on diversity in clinical trials.
Content Solutions for MDR & IVDR Readiness
Technology Virtual Summit: November 2020
Automation technologies, strategies, and applications to address the impact of dramatic regulatory change
Artificial Intelligence in Life Sciences – Latest Developments Presented by Industry Leaders
Thursday, September 24, 12:00 PM EST
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.
Part 4: Clinical Trials and COVID-19 Remote Investigator Meetings
July 21, 2020
TransPerfect's Trial Interactive presents Part 4 of the Clinical Trials and COVID-19 webinar series with industry-expert Penelope K. Manansco to discuss the best strategy for remote investigator meetings.
Driving Strategic Change – The Evolution of GCs in Pharma
June 11, 2020
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.
Part 3: Clinical Trials and COVID-19 Adapting to Rapid Change
April 28, 2020
TransPerfect's Trial Interactive hosted Part 3 of the Clinical Trials and COVID-19 webinar series with representatives from a Sponsor and Site to discuss how they are helping their team members navigate this new landscape.
Part 2: Clinical Trials and COVID-19: Converting to Remote Trial Management – How to Get Started
April 23, 2020
TransPerfect’s Trial Interactive will be hosting a webinar with the CEO of MANA RBM for organizations considering making the transition from largely manual, paper-based processes to complete remote trial management.
Part 1: Clinical Trials and COVID-19: Situation Now, Its Challenges, and the Future
April 14, 2020 | 11:00 AM ET
TransPerfect Life Sciences will be hosting an interactive session with industry experts from Ferring Pharmaceuticals, Merck, and Clinical Innovation Partners (ex Pfizer).
Simplifying Clinical Trial Training Management
December 20, 2019
Marc Gracieux, GlobalLearn Product Manager
Lay Summary Development Navigating the Trail of Regulatory Writing
October 22, 2019
Kelsey Brown, Medical Writing Manager, TransPerfect
The Right eTMF Approach for You: Sponsor or CRO-Owned eTMF?
June 18, 2019
Laurel-Ann Schrader – Associate Director, Clinical Operations, TransPerfect Trial Interactive
Mof Osei – Senior Director, Records Management Compliance, Worldwide Clinical Trials
Le Thu Nguyen – Senior Clinical Documentation Manager, Sponsor
Rethinking Medical Device go-to-market clinical strategies in the light of the new European MDR
May 2, 2019
Meghan McCrea – Regional Director, TransPerfect Life Sciences
Adam Steadman – VP Clinical Development, Business Unit Head, Medical Devices & Diagnostics at Syneos
Content Requirements Under MDR…And What You Can Do About It
June 27, 2019
Marc Miller - Division President, TransPerfect Medical Device Solutions
Keith Morel, PhD – VP of Regulatory Compliance / Principal Consultant Qserve Group


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