AppsAccelerate for Med Device is a suite of prebuilt solutions purpose-built for medical device manufacturers to streamline compliance, modernize legacy systems, and gain actionable insights. Built on Oracle Cloud, these accelerators offer faster time-to-value, enabling organizations to reduce risk, optimize operations, and maintain agility in a regulated environment. From GxP validation and Sunshine Act reporting to PLM transformation and gross-to-net accuracy—AppsAccelerate for Med Device helps you meet today’s compliance challenges without slowing innovation.
Enable risk-based, scalable validation for Oracle Cloud applications with AppsAccelerate for Med Device: Validation as a Service. Designed to support SaaS deployment models, this solution aligns with internal SOPs and GxP requirements, leveraging Oracle certifications to reduce overhead. Stay compliant with structured change control, proactive release readiness, and seamless integration into your quality system—without slowing down innovation.
Migrate from Agile to Oracle Cloud PLM with confidence. This conversion framework is tailored for medical device companies, supporting GxP alignment, regulatory compliance, and complex data needs. Reduce system complexity, extend the digital thread, and gain a unified experience across quality, supply chain, and product development—all while meeting standards like ISO 13485, CFR 820, and CFR Part 11.
Automate gross-to-net calculations and gain transparency across revenue deductions with a solution built for medical device and pharma companies. This accelerator delivers accurate accruals, streamlined reporting, and strategic insight into pricing and reimbursement. Quickly deploy prebuilt configurations to enhance compliance and drive smarter financial decisions.
Simplify and automate HCP spend tracking with AppsAccelerate for Med Device: Sunshine Act Reporting. Capture detailed spend by category, product, and activity while leveraging a purpose-built data model and real-time analytics dashboards. Meet regulatory requirements with confidence, reduce manual intervention, and gain visibility into compliance risks—fast.