Our Scientific Applications Support team has assembled a list of frequently asked questions to help you find answers quickly. Filter using one or more categories to focus on specific topics, or use the search bar to perform a text search.
IDT is prepared to support you with required information based on use, clinical program phase and modality. These include but are not limited to drug master files, site master files, site audits, and so on. Contact us for a consultation to discuss your regulatory needs.