Regulatory Document Management Fact Sheet
Creating and managing regulatory submissions becomes more challenging every year. The size of US NDAs continues to expand, with some containing in excess of 500,000 pages of documents and data. Then there is the sheer volume of submissions – managing all of the amendments, supplements, and variations needed to maintain and expand the product portfolio across regions and countries. Ever-tightening submission time frames amplify the cost of mistakes and rework. On the back end, documents intended for electronic submissions must be authored to a higher standard.
NextDocs' pre-configured solution for managing submission documentation addresses these key challenges to deliver a compliant, user-friendly solution while minimizing the demands on your already overtaxed business and IT users.
Get unlimited access to:
Enter your credentials below to log in. Not yet a member of Clinical Leader? Subscribe today.