360° fme Professional LSSS Services

We ensure a seamless implementation of the OpenText Documentum for Life Sciences Solution Suite and support you with the alignment on the business process – also on a global scale!

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Webinar: How to Migrate Your Content to the LSQM System with migration-center

On-demand Webinar

How can you migrate your data to the LSQM module? What are the challenges involved and how can you overcome them? Find out more in our on-demand webinar, which also includes a demonstration.

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OpenText Enterprise World 2018

July 10-12, 2018 in Toronto

Meet our global team from the US, Germany and Romania in Toronto to learn how to benefit from our consulting and services for OpenText Documentum and our efficient content migration services. We are looking forward to meeting you!
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A Solution Tailored to Your Needs: On Premise or in the Cloud

We offer a complete range of services that provide flexibility, agility, and security, which in turn allows us to create solutions that are tailored to your needs.

Do You Want to Expand Your LSSS?

We and fme-Partner offer a large number of expansions. These include Widgets (e. g. Dimension Viewer & Simplified User Interface) as well as an integration of Microsoft SharePoint, Extedo eSUBmanager and Sparta Trackwise.

    OpenText Documentum Life Sciences Solution Suite
    Turnkey solutions, standardized processes, and seamless information sharing

    Are you looking for a holistic Life Sciences Solution Suite to meet regulatory compliance requirements, increase efficiency and productivity, balance access, control and localization as well as securely collaborate across the enterprise?

    The OpenText Documentum Life Sciences Solution Suite (LSSS) is a basic framework for document management applications that optimizes access, management, and exchange of information in life sciences companies, making information silos a thing of the past.

    Your benefits

    • Improved business productivity and efficiency
    • A trusted, compliant and scalable ECM-/Documentum platform that is cloud ready
    • Integrated, easy to configure purpose-built solutions with intuitive user interface
    Life Sciences Solution Suite Modules

    The pre-configured, integrated solutions are based on best practices for this industry branch and are available as specific business modules for standardized business processes for the business areas of quality assurance, clinical and non-clinical research, and regulatory issues.

    Electronic Trial Master File

    Optimal planning, collection, and coordination of clinical studies that can be reviewed at any time

    You can improve and review your study’s structure by quickly compiling the necessary documents with the Electronic Trial Master File solution. Collect and synchronize documents with sponsors, clinical contract research organizations, and others. The Solution Suite also enables a real-time insight into the process for capturing study documents and guarantees successful audits thanks to a system that can be reviewed at any time.

    Research & Development

    Quicker creation, review, and approval of documents subject to compliance

    This business model ensures that all documents are completed for submission and have undergone a review and approval process based on industrial standards. They improve authors’ productivity and simplify the review process. Furthermore, the solution enables a quick document search to compile your submission documents more quickly.

    Submission Store and View

    Ensure a seamless overview of all regulatory activities

    The Submission Store View Solution simplifies the search and request of archived submissions and the documents connected to it. Import regulatory submissions in eCTD, NeeS, or paper format and store them with the accompanying communication. This solution provides you with a comprehensive insight into your regulatory activities. You can easily access correspondence on products or submissions.

    Quality & Manufacturing

    Simplified creation, coordination, review, and approval of GMP documents

    This user-friendly Solution Suite ensures adherence to compliance regulations for good manufacturing practices (GMPs). Review quality and manufacturing documents and automated, company-wide workflows. Manage industry-specific processes and guarantee appropriate change procedures. This business model allows documents to be quickly and easily shared even with global users.

    Our 360° fme Professional Services

    We developed our 360° fme Professional Services based on our 15+ years of experience working with ECM for life sciences and collaborating with global customers as well as medium-sized manufacturers. We will draw on our industry and content migration expertise, proven Prince 2-based project management methodology, and Roll Out Support (module-by-module vs. complete suite) to make your project a success. We are happy to help you, whether you require a local solution or a solution operated from a private, public, or hybrid cloud.

    LSSS Lifecycle Service

    We will help you throughout the entire lifecycle, from process analysis, solution development, installation, and configuration through to adaptation, integration, global operation, and round-the-clock support.

    OpenText Documentum Content Migration Service

    Our migration-center is the bridge between your content in file or legacy systems and the OpenText Documentum Life Sciences Solution Suite. Understanding the target Opentext Documentum object design based on the principles of the DIA reference model is one of the core expertise areas of fme for migrations. Further, fme’s migration-center software combined with best practice experience qualifies fme as first choice for Life Sciences companies to support complex and critical migration projects.


    In-Place-Migration

    For specific migration paths with the target of D2 based systems, migration-center supports a so called in-place migration to streamline the process. Object IDs and audit trail entries remain during this conversion.


    migration-center Validation Package

    The migration-center Validation Package is a new and exclusive approach based on best practices that simplifies the verification process and therefore reduces the time the business is involved in migration projects. This additional package for migration-center projects consists of two basic components: A collection of needed document templates and consulting services to adapt the templates to the individual client validation needs.

     

    Our fme LSSS Services at a Glance

     

    Now, with fme and the OpenText Documentum LSSS, you are embracing the future with unprecedented efficiency, agility, document control and compliance that‘s key to getting products to market ahead of the competition. We look forward to your challenge!