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Optimizing growth in global markets requires operating at a broad scale, without losing sight of local regulations for design, quality, and commercialization.
Propel’s Quality Management System (QMS) simplifies compliance by consolidating market-specific documents and maintaining audit trails for design changes and quality issues.
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Digital FDA Submissions help regulatory and quality teams efficiently manage the entire process with the FDA. Ensure compliance and improve audit readiness by connecting early design to customer feedback and regulatory reporting.
Quickly and accurately resolve customer complaints and QA investigations to improve product safety and customer loyalty. Fully integrate to case management systems to leverage customer insights.
Quickly train and certify employees and suppliers on regulatory and safety changes. Assign site-specific and role-specific requirements to meet local regulation and safety policies.
Achieve compliance faster using configurable templates and digital submissions.
Gain efficiency and reduce errors using automated workflows and reports.
Achieve and maintain compliance across domestic and global markets to secure new revenue sources.
“We needed a solution that could adapt to us versus us adapting to them. With Propel we can mistake-proof our processes to gain business efficiencies and at the same time ensure compliance.”
– Brent Lewis, Director of Enterprise IT Quality and Compliance Systems
See how you can speed your products to local and global markets
without exhausting your efforts.
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