When ZAI began working with FDA more than 20 years ago, paper records were the norm. Since that time, we’ve been developing efficient and innovative solutions to help manage electronic document processes. ZAI has worked behind the scenes to enable drug submissions to move efficiently through FDA’s systems, while increasing public safety through information management. 

We built the systems that are the crux of the drug submission process. We also manage document creation and delivery via shipment and courier, as well as provide storage, retrieval, archival, and destruction. For this highly-regulated industry, enforcements are always changing, and we’ve delivered the agility and subject matter expertise needed. As FDA has grown exponentially over the years, ZAI has been there to serve its system design and development needs.