Regulatory Submission Software OpenText Core for Regulatory Plans
Simplify planning to accelerate health authority submissions
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OpenText Core for Regulatory Plans overview
Life Sciences companies must file regulatory submissions with regional health authorities to market new therapeutic products and maintain product registration. Regulatory professionals navigate through complex and evolving regulatory requirements as they work with stakeholders.
OpenText™ Core for Regulatory Plans simplifies submission planning and assembly with intuitive wizards, extensive automation and streamlined information architecture. The SaaS solution offers the agility and cost efficiency to meet regulatory obligations, even in the most complex regulatory scenario.
OpenText Core for Regulatory Plans features
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Create submissions
Leverages an intuitive wizard guides the set-up hierarchical eCTD structure, automatically assigning document control, resources and due dates to create regulatory submissions in electronic format.
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Manage regulatory events
Ensures global compliance by creating and managing regulatory events across regulatory jurisdictions within the regulatory submission process.
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Identify impacted submissions
Allows users to rapidly and accurately identify registrations and applications impacted by a regulatory event.
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Track progress
Offers realtime visibility into submission status by region and tasks to provide a global perspective across the regulatory organization.
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Notify team members
Keeps teams focused on submission priorities with tasks and email notifications that help coordinate across clinical, quality, manufacturing groups.
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Secure access
Offers regulatory submission management software with secure access to authorized users, continuous new capability delivery and seamless onboarding and upgrading to minimize deployment risk.
OpenText Core for Regulatory Plans benefits
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Speed to market
Reduce complexities by automating submission planning and assembly tasks with electronic regulatory submissions software.
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Improve efficiency
Reuse content by connecting to submission and authoring processes managed in OpenText™ Documentum™ for Life Sciences.
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Save time and reduce errors
Replace manual processes with automation and smart features.
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Risk mitigation
Track global regulatory submissions status and progress through dashboards and notifications to mitigate timeline risks.
OpenText Documentum for Life Sciences
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OpenText™ Documentum™ for Research and Development
Accelerate creation, review and approval of submission documentation
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OpenText™ Documentum™ Submission Store and View
Obtain a 360-degree view of regulatory activity and improve compliance of archived submissions
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OpenText™ Documentum™ for Quality and Manufacturing
Control critical quality documentation, streamline and automate processes with compliance
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OpenText™ Documentum™ for eTMF
Navigate complex clinical trial processes and take complexity and risk out of trial related document management
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OpenText™ Content Cloud™ for Life Sciences
Add new efficiencies to the productivity and governance capabilities of OpenText Documentum for Life Sciences
