Navitas pharmaREADY DMS is a web-based Document Management System that automates and seamlessly manages your document management process to ensure compliance by having demonstrable control of your content. The functionality built into the pharmaREADY Document Management system stems from a deep understanding of the requirements for meeting and maintaining compliance with FDA 21 CFR Part 11 and other international standards.

pharmaREADY eDMS meets the needs of these types of Life Sciences organizations including:

  • Pharmaceutical
  • Biotech
  • Contract Manufacturers
  • Medical Device
  • Generics
  • Animal Health
  • Clinical Research Organizations

pharmaREADY DMS manages the entire content lifecycle process and gives you the tools to securely manage a wide range of business documents, including those related to regulated compliance and submission dossiers. The Navitas team brings a wealth of experience from life sciences professionals and technology experts, and applies that expertise to a product vision with the goal of reducing the burden of business problems experienced by Life Sciences organizations.

Business Problem

Existing Scenario at Life Sciences Organization

pharmaREADY Document Management System Advantage

Installation & Configuration

Installation is often made more complex by customizations to the out-of-the-box tool.

Typical installation cycle is less than a week

Total cost of ownership
(including maintenance & support)

Expensive & complex licensing

Extremely attractive pricing and a simple licensing model

  • Enterprise Licensing
  • Small-Midsized enterprise licensing
  • On-Demand / hosted model

Ease of Use

Heavily customized, large-scale enterprise DMS applications are often made more complex to use from an end-user and administrative perspective

The fundamental design philosophy of pharmaREADY DMS is primarily based on providing a rich user experience and enhancing product usability

Small-to-mid size company need for Regulatory compliant DMS products

Most large enterprise scale products don’t make sense for smaller numbers of users since they require significant configuration and “care and feeding.” Other tools limit the number of documents in the docbase.

pharmaREADY DMS provides the required functionality without being too large or limiting the number of documents you can work with

Navitas pharmaREADY DMS provides the features and functions needed to securely and efficiently manage all regulated content through the entire content lifecycle.

pharmaREADY DMS is a fully 21 CFR Part 11 compliant document management solution leveraging Microsoft technologies. pharmaREADY DMS is designed specifically for the management of all regulated content as well as other documents your enterprise creates, consumes, and maintains.

pharmaREADY DMS is available as an independent product or is easily tightly integrated with other pharmaREADY products including pharmaREADY eCTD and pharmaREADY TRMS, thereby providing seamless visibility into the entire regulatory document management lifecycle, from document creation all the way to regulatory submissions.

02
Nov2016

BioVectra chooses pharmaREADY for eCTD Solution

BioVectra has chosen pharmaREADY for its eCTD requirements. BioVectra, located in Canada, manufactures ingredients for global...

05
Oct2016

Navitas at DIA's 10th Annual Forum for Qualified Persons...

Navitas Principal Jeffrey Ho will present “Efficient content management for the compilation and management of the...

12
Jul2016

Navitas Celebrates 100th pharmaREADY customer

pharmaREADY is Navitas’ intuitive and easy to use, fully integrated, regulatory compliant, web-based suite comprised of modules...

16
Oct2015

Navitas Introduces Innovative Regulatory Process Outsourcing Model

The workload for regulatory functions of pharmaceutical companies has continued to increase in recent years ...