Sold by: Successive Digital
Streamline drug approval processes with Generative AI for regulatory compliance and documentation in the life sciences industry. Successive Digital’s Gen AI-powered document compilation and formatting enables automated regulatory submissions, ensuring adherence to guidelines, regulatory assessment, and post-market surveillance.
Overview
Leverage Generative AI to streamline the preparation of regulatory submission documents for your life sciences business use cases. Our Gen AI-powered solutions help you create comprehensive standard operating procedures (SOPs) and clinical trial protocols, ensuring consistency and compliance.
Our solution efficiently manages, archives, and retrieves regulatory documents,It also offers seamless data management by integrating clinical trial data from multiple sources with AWS’s data lakes and integration services. Additionally, we deploy AWS’s machine learning models to access and analyze global regulatory changes, keeping you ahead of evolving requirements. Let us use Generative AI to help you enhance your regulatory compliance and documentation processes.
Our Generative AI solutions for Lifesciences look like this:
Automated Regulatory Submissions Policy and Protocol Generation Document Management and Storage Compliance Monitoring and Reporting Training and Certification Management Risk Management and Assessment Regulatory Intelligence and Updates
Highlights
- Compile and format regulatory documents for drug approval
- Ensure regulatory compliance
- Generate Clinical Trial Protocols (SOPs)
Details
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Delivery method
Deployed on AWS
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Pricing
Custom pricing options
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Support
Vendor support
24*7 premium support services. contact sahaya@successive.tech