Services

Solution Overview

Planning a submission includes orchestrating all of the deliverables, approvals, resources and timelines for a submission. And every global product has over 10 million regulatory data points. arivis can transfer our experience with a vast variety of submissions.

Solution Overview

The process of preparing submission content for the electronic submission process is an intricate and precise endeavor. arivis has the tools, resources, and processes in place to provide you with timely and accurate submission documents.

Solution Overview

Preparing documents for submission can be a challenging undertaking. Making documents consistent, per-guidance, and reviewer ready takes a detailed and rigorous process.

 

Solution Overview

Achieving and maintaining compliance with regulatory requirements is one of the most important goals for a pharmaceutical company. At the same time it is difficult to stay on top of all requirements, as it requires a lot of investment in terms of time and resources.

Solution Overview

Existing internal resources are overloaded with the additional task of product data maintenance, specifically in the dynamic environment of the pharma industry with mergers and acquisitions of companies or product portfolios.