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Clinical Trial Disclosure Services

Clinical Trial Disclosure Services

IQVIA
Pages 2 Pages

This fact sheet covers IQVIA’s services for meeting global clinical trial transparency requirements. Support includes protocol registration, results reporting, redaction/anonymization, and plain language summaries. IQVIA monitors evolving regulations like EU CTR and Health Canada initiatives, ensuring compliance and efficiency. Expertise includes membership in EMA and cross-industry working groups. Services span trial start-up, maintenance, and completion, helping sponsors navigate disclosure obligations confidently.

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