Ep 88. How to Move Beyond Medical Translation into Regulatory-Ready Linguistic Validation with Nur Ferrante

In this week's episode of Freelancer Training, we’re joined by Nur Ferrante, a seasoned linguistic validation consultant, to explore just how medical translators can evolve into indispensable players in the clinical trial ecosystem through the niche field linguistic validation.

🔍 What You’ll Learn:

✅ Master the Full Linguistic Validation Lifecycle
Nur breaks down each phase of the linguistic validation process—translation, reconciliation, back translation, cognitive debriefing, harmonization and final proofreading—drawing on real-life examples and industry best practices aligned with ISPOR and EMA/FDA guidelines.

✅ Optimize Quality and Compliance in Clinical Trials
Discover how high-quality linguistic validation safeguards patient safety, upholds data integrity, and supports regulatory approval. Nur shares how to proactively resolve challenges in cultural adaptation, terminology consistency, and patient comprehension to meet global standards in clinical research.

💡 Who This Episode Is For:

• Medical translators seeking to expand into high-value clinical trial work
• Language professionals aiming to build regulatory knowledge and skills
• Freelancers looking to position themselves as compliance-oriented experts

🎧 Listen now to gain insider insights into one of the most specialized and in-demand areas of clinical translation—and learn how you can position yourself as a trusted partner in the life sciences sector.

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