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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Leveraging Social Media for Patient Recruitment in Clinical Trials
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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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International Women's Day: Embracing Equity in Life Sciences

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IMP Labeling EUCTR
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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). ...

COA Patient Voice
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Hearing the Patient Voice Through Technology and eCOA

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COA migration
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3 Benefits of Centralizing Global Content Solutions for Regulatory Teams

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EUCTR Considerations
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Assessing Readiness for EU Clinical Trials Regulation (CTR): Five Points to Consider

Assessing Readiness for EU Clinical Trials Regulation (CTR): Five Points to Consider...

Investigational Medicinal Products
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Investigational Medicinal Products: Labeling Changes and Their Implications

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Pharmacovigilance (PV) & Safety Automation
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3 Automation Outcomes for Pharmacovigilance and Safety Teams

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Electronic Labeling
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Benefits of Electronic Labels: Investigational Medicinal Products

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DCT
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Decentralized Clinical Trials | TransPerfect Life Sciences

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patient diversity
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Lack of Diversity in Clinical Trials: A Conversation

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plain language summary
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Plain Language Summary Requirements for Clinical Trials

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clinical trial patient diversity
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Reaching Diverse Patient Populations to Drive Inclusivity in Trials

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intellectual property (IP)
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Intellectual Property (IP) Strategies to Consider for Life Sciences Start-Ups

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Patient Recruitment Diversity and Inclusion
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Connecting with Diverse Patients: How Call Centers Can Improve Patient Recruitment and Retention

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electronic product information
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Electronic Product Information – Everything You Need to Know

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COA Migration
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3 Benefits of Centralizing Global Content for eCOA Migration

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pharma digital marketing
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Pharma Digital Marketing: Trends for Customer Engagement

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Literature Monitoring
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Why Automate the Literature Monitoring Process?

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patient engagement in clinical R&D
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Driving Patient Engagement in Medicine Development and Decision-Making – Challenges and Opportunities

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Patent priority date
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Leveraging the Patent Priority Date: A Life Sciences Focus

This TransPerfect Life Sciences blog post provides insights into the strategic importance of patent priority dates in the life sciences sector. ...

digital health
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Digital Health’s Role in Improving Patient Engagement

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CCMS
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4 Ways a CCMS Can Help Medical Affairs Achieve Global Content Reuse and Omnichannel Delivery

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AI for pharmacovigilance (PV)
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Leveraging Artificial Intelligence (AI) in Pharmacovigilance

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