Our research shows that ‘getting it right’ is a leading concern of regulatory professionals. IQVIA’s Productivity Tools make authoring and PDF publishing easy, fast and efficient. And our validation tool ensures that what you submit is in technical compliance with health authority requirements.
Select the right shell document for your regulatory work with IQVIA Regulatory Templates. Right down to the specific region, module and document type required.
Specifically designed for the life sciences industry, IQVIA Regulatory PDF Tools provide customers with a simple, practical way to prepare PDF documents for submission.
IQVIA eSubmission Validator verifies electronic Common Technical Documents (eCTD) and Non-eCTD Electronic Submissions (NeeS) documents, ensuring compliance with regional and ICH specifications and requirements prior to dispatch.