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FAQ updated for the CTIS training programme

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FAQ updated for the CTIS training programme

By SaadMay 15, 2026No Comments

Home » FAQ updated for the CTIS training programme

The European Medicines Agency (EMA) has published an updated FAQ for the Clinical Trials Information System (CTIS) Training Programme, Module 16: Supervise a Clinical Trial – Inspection records.

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PHARMYA is a French based company, dedicated to providing Pharmacovigilance services. Its mission is to support the pharmaceutical industry, biotechnology companies, research centers and their service providers in their efforts to comply with international Pharmacovigilance regulations.

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