For Life Science, by Life Science professionals:
It takes 12 years on average for an experimental drug to travel from the laboratory to the medicine chest. Only five in 5,000 compounds that enter preclinical testing will actually progress into human clinical trials, and of these five, only one is likely to be approved by the regulatory authorities.
Experts forecast that the cost of producing a successful drug could top $2 billion by 2010 unless the pharmaceutical industry can identify new and better ways to improve efficiency and effectiveness of drug discovery and clinical trials. Cost pressures are enormous, even on those drugs already in the pipeline. In today's high-paced world of drug development, each day a new drug is not on store shelves can mean $1 million or more in lost revenues.
Doublebridge Technologies with decade over experience in servicing the Global top 20 Pharmaceutical companies understands the time constrained business processes and offers a wide range of innovative solutions for Life Science Industry. DoubleBridge invests the domain expertise and technical know-how to address some of the prime challenges in Life Sciences.
Be a start up, medium sized business or Large Pharmaceutical our array of products are made for every purse and purpose. Some of the key areas covered by our product line include
- Regulatory Document Management
- eSubmissions in SharePoint
- eCTD and NeeS Viewing Solutions
- Submission Tracking and Archiving
- Regulatory Event Tracking
- Regulatory Auditing
- Regulatory Requirements Management
ROSETTA Phoenix eCTD Viewer
ROSETTA Phoenix is designed for the viewing and reviewing regulatory submissions prepared in Electronic Common Technical Document (eCTD) format standard used by life sciences industry and regulatory authorities.
ROSETTA Pyramid - Submissions Tracking and Archive
ROSETTA Pyramid is the retrieval solution based on EMC Documentum. It is an active archive of a submission (paper or electronic) for immediate retrieval. It provides powerful search tools and immediate access to submission documents offering the best defense in the event of an audit, litigation and legal discovery. With the advent of eCTD, the lifecycle of a document isn't final after submission. Reference to a document and lifecycle operations may occur anytime. This changes the notion of an "archived" document as something simply filed away in case it is needed; archived documents must be available for immediate retrieval. ROSETTA Pyramid provides automatic indexing for eCTD submissions and includes an embedded version of ROSETTA Phoenix to facilitate the navigation of those submissions and the immediate retrieval of their content. Combined with our migration service, ROSETTA Pyramid can be your single system for all your company's submission records and documents.
OrniPoint - SharePoint based Life Science Suite:
OrniPoint is a SharePoint based, off the shelf solution / tool kit that will address all of the challenges faced with content management in regulated industries. Completely integrated with SharePoint framework, OrniPoint lowers your total cost and maximizes your benefit. OrniPoint guarantees minimum deployment, development time and less transition time from implementation to business as usual.
We have leveraged our rich domain knowledge by servicing some of the world's largest Documentum based systems and energetic technology team to produce a compelling SharePoint Suite for Regulated industry which includes:
OrniPoint Falcon - The SharePoint-Based Regulatory Document Management Solution
OrniPoint Griffin - The SharePoint OmniConnector for Documentum, Lotus Notes, and eRoom
OrniPoint Nest - The SharePoint-Based Program Management Library for Life Sciences
OrniPoint Branta - The SharePoint-Based Virtual Document Manager
OrniPoint Jay - The SharePoint-Based Long-term Deliverables Scheduling Tool