Cloud-Based Task and Document Management Platform
Effortless Control of Your Clinical Supply Operational and Associated Data Workflows
PROMAP is our proprietary cloud-based task management and data-sharing platform, designed to simplify to most complex supply chain challenges. It provides a centralized, real-time solution for storing, sharing, and reviewing critical regulatory and batch certification data and documents.
From manufacturing and testing to distribution, PROMAP offers a clear framework that allows you to:
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Visualize and manage your supply chain documents and tasks in real-time.
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Identify and address challenges early to prevent costly delays.
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Ensure on-time approval, release, and delivery of investigational products.
Streamlined Supply Chain Task & Document Management
PROMAP is more than just a platform, it’s part of PRONAV Clinical’s boutique consultancy service. We work closely with you to create custom workflows and strategies that fit your unique project needs.
Comprehensive Supply Chain Visualization
PROMAP utilizes handcrafted flowcharts to map your supply chain from start to finish, highlighting regulatory milestones, compliance requirements, and critical documents. This proactive approach eliminates guesswork and keeps your project on track.
Secure and Compliant Data Management
PROMAP ensures the integrity of your data with 21 CFR Part 11 and EU Annex 11 compliant secure storage and processin. Documents are protected in a centralized, compliant environment that allows seamless sharing and collaboration among your team and PRONAV Clinical experts.
Key Features of PROMAP
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Custom Framework Design
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Tailored flowcharts to outline every stage of your supply chain.
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Real-time tracking of tasks and milestones to ensure nothing is missed.
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Real-Time Collaboration and Visibility
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Centralized access for your entire team to monitor progress and address issues as they arise.
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A single-point platform for qualified persons (QP) to review data efficiently and support batch releases.
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Streamlined Document Management
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Secure storage and easy transfer of sensitive regulatory documents.
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Task management tools to accelerate approvals and avoid bottlenecks.
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Proactive Risk Mitigation
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Early identification of challenges to prevent delays.
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The system is fully qualified (21 CFR Part 11 and EU GMP Annex 11).
CAPABILITIES
PROMAP supports the transfer, storage, review and approval of all supply chain documentation, including:
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Discovery and Framework Design
We begin by working with your team to understand your specific needs and challenges, creating a custom roadmap and process flow.
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Platform Customization
PROMAP is tailored to your project, incorporating unique workflows, regulatory milestones, and document management tools.
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Real-Time Monitoring
Your team gains full visibility of tasks, deadlines, and data, with updates and notifications ensuring nothing falls behind.
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Data Security and Compliance
All documents are stored in a secure, pharma-qualified U.S database, ensuring regulatory compliance and data integrity.
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On-Time Delivery
With streamlined workflows and proactive oversight, PROMAP keeps your supply chain moving efficiently to meet clinical trial deadlines.
The PROMAP Process
Partner with PROMAP for Seamless Project Management
Whether you’re managing a single batch or a multi-site trial, PROMAP provides the tools and expertise to simplify your clinical supply chain and regulatory processes. With its combination of cutting-edge technology and boutique consultancy, PROMAP ensures your projects are completed on time, with precision and compliance at every step.