Submission Management
Regulatory operations Submission involves the compilation, preparation, and submission of regulatory documents to health authorities or notified bodies to support the approval and maintenance of products.Our solution has ability build, manage, publish, validate and archive regulatory dossiers. Our solution areas include:
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Document Collection: Regulatory operations publishing functionality manages collection of documents from various teams (or external systems we can connect to). These documents can be in various formats, such as Microsoft Word or Adobe PDF. Our built-in document format automation will QC and Auto-Fix documents as per country specific requirements
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Document Preparation: The collected documents are then prepared according to the regulatory requirements and guidelines. This involves formatting, reviewing, and editing the documents to ensure consistency and accuracy. And our tool will handle all these steps as part of document automation process to save your time.
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Submission Tracking: Regulatory operations publishing also involves tracking the status of the submission with the regulatory authorities. This involves monitoring for acknowledgments, requests for additional information, and other communication.
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Life-Cycle Updates: Once the submission has been approved, regulatory operations publishing also includes updating the regulatory authorities with any changes to the product, such as label updates or manufacturing changes. Our detailed life-cycle management handles both document level operations and correspondence aspects
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Compliance: Regulatory operations publishing must comply with regulatory requirements, such as the International Council for Harmonization (ICH) guidelines, regional regulations such as FDA regulations, EU MDR and and your internal rule books as well as standard operating procedures (SOPs).
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Collaboration: Regulatory operations publishing requires collaboration with internal and external stakeholders, including regulatory affairs, quality assurance, medical affairs, and clinical development teams. Our built-in submission project management and collaboration ensures that the regulatory submission is accurate, complete, and compliant.
Overall, regulatory operations Submission is critical and our solutions help ensure save time/costs, cut cycle time and maintain compliance.
Dossier Build & Publish
Our solution enables you to readily build, view, validate and publish compliant submissions based on Standard country formats. Countries with custom submission requirements and all life cycle submissions of different applications for various countries. Some Highlights include:
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Pre-built country publishing Plans
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Custom Submission plans using our Template Management functionality
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Custom Submission plans using our Template Management functionality
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Cross-country dossier linkages
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Different outputs (XML, Zip, PDF)
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Manage Life cycle easily
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Integrated with your current tools/systems
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