Resources | TransPerfect Life Sciences

Thought Leadership

Health Canada's Transition to XML: What Regulatory Teams Need to Know

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Health Canada’s shift to XML Product Monographs starts July 2025. Learn what regulatory and compliance teams need to do now to stay aligned and submission-ready. |

In a continued push toward modernization and transparency, Health Canada has entered the next phase of its digital transformation with a mandate requiring the use of advanced extensible markup language product monograph (XML PM) files. This change builds on earlier initiatives and introduces new filing requirements that will impact how regulatory, compliance, and medical writing professionals prepare, submit, and manage product monograph (PM) content. If your team is...

Web Localization Playbook for Life Sciences

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The Total Economic Impact of TransPerfect GlobalLink for Life Sciences

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Ask an Expert Office Hours: Website Localization for Patient Recruitment - 4/24/25

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An Overview of Generative AI and Machine Translation for Life Sciences

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Blog

The Role of Qualitative Interviews in Ensuring a Patient-Centered Approach to Clinical Trials

Discover how qualitative interviews (CE, CD, PE, EI) enhance clinical trials. Learn best practices for conducting patient-centered interviews and ensuring accurate, meaningful data. Trust TransPerfect Life Sciences for expert interviewers and top-quality translation and...

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The Future of eCOA and Wearable Devices

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The C3 Summit: Boston Recap

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How Medical Writing Can Drive Patient Engagement

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Centralizing Global Content Solutions for Medical Affairs

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The C3 Summit: San Francisco Recap

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Overcoming 5 Challenges of Implementing eClinical Technologies

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Centralizing Global Content Solutions for Patient Engagement Teams

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What Are Unitary Patents and What Do They Mean for Life Sciences Companies?

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The Quality Review of Documents (QRD) v9.0 for Veterinarians: A Step Toward Better Care

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Leveraging Social Media for Patient Recruitment in Clinical Trials

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International Women's Day: Embracing Equity in Life Sciences

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IMP Labeling: EU CTR Transition Considerations

The blog post explores the critical aspects of transitioning Investigational Medicinal Product (IMP) labeling from the EU Clinical Trial Directive (EU CTD) to the new EU Clinical Trial Regulation (EU CTR). ...