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Dear GlobalSubmit Customer
GlobalSubmit 2010 is officially in beta and we cannot wait to share our new products with you!! Sign up to see our brand new functionality and the following product modules:
- VALIDATE is better than ever with PDF checks and several new errors that the FDA will be using
- REVIEW will blow you away... wait until you see what you can do now
- CROSS-CHECK was designed with your Reg Ops team in mind - come see how to shave a few days of your submission timeline
- PUBLISH is innovative and cost-effective. And it integrates seamlessly with REVIEW and VALIDATE!
Join us for a demonstration by Kathie Clark, our director of Professional Services. She will be happy to show you how we have listened to your feedback and used it to produce our best products yet.
Please note, registration is required in advance and you will need be on the entry list to attend.
We cannot wait to see you online and to give you a preview of the GlobalSubmit 2010!!
Best regards,
Laura Wright,
GlobalSubmit Account Manager
Hosted By
GlobalSubmit Demonstration Team
GlobalSubmit is a products and services company that provides transparency in regulated healthcare products. The U.S. Food & Drug Administration and leading Life Sciences companies use our flagship applications, REVIEW™ and VALIDATE™, to review and validate electronic submissions. GlobalSubmit’s thought leaders lead international efforts, constantly working with industry and government agencies to standardize product and study information. The company is headquartered in Philadelphia, Pennsylvania.
