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NextDocs 6: The New Enterprise Standard for Regulated Content Management
Date:4/26/2013

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  • Delivers quick start capabilities via software-as-a-service
  • Provides pre-configured workflows built using industry-proven practices
  • Offers scalability and resources to develop and grow programs
  • Leverages proven results from leading life sciences companies
  • Carries a lower total cost of ownership (TCO)
  •  

    "We've leveraged our experience across more than 100 customer deployments to design NextDocs 6.  Now, customers can take advantage of a next generation technology platform, while also embedding  industry-proven best practices," said Satwik Seshasai , Chief Technology Officer at NextDocs. 

    The advantages of the pre-built configurations, compliance engine and redefined mobile experience are extremely beneficial in a clinical trial management environment.  NextDocs Trial Exchange solves the challenges that life sciences companies face in managing clinical documents in an increasingly global and partner-enabled environment.  The solution allows remote trial site staff to contribute documents to an established eTMF work stream, receive and complete tasks generated by the sponsor, view document statuses, and retrieve documents on demand using tablets and smart phones.  As a result, it can reduce the time and cost of trial management, improve collaboration with investigators, and strengthen security and compliance.

    The company also announced the availability of NextDocs QuickStart, an all-inclusive, cloud-based offering for companies looking to get started with electronic regulated content management.  QuickStart includes the pre-configured software, implementation services and support required for a successful deployment.  The solution and cloud infrastructure are pre-validated, which speeds deployment and lowers costs.
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    SOURCE NextDocs
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