Vetter Pharma

Regulatory support

Regulatory support for your clinical trials

Our experts provide the guidance, insight, and Vetter process documentation you need to prepare a Common Technical Document (CTD) for clinical trials of your injectable drug product.

Quality and compliance from the first step

Efficiently and successfully navigating regulatory pathways is a critical step in keeping your clinical development cycle on time and on budget. In addition laying strong regulatory groundwork during your clinical trials can set your product up for even greater success at key future milestones in your product’s life cycle.

Our Regulatory Affairs team is here to provide the regulatory support to keep your product’s timelines on track – from your first clinical batches, to Phase 3 and beyond.