Today’s stringent, global regulatory environment is exacting. And staying in compliance is an on-going, time-consuming series of activities.
IQVIA Productivity Tools make it easy to rapidly prepare, publish and validate eCTD and non-eCTD electronic submissions to regulatory authorities, giving your regulatory staff valuable time back for higher-level activities.
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.
Reimagine regulatory service delivery.
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.
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