Solution
ICH CTD Automation – Streamlining Regulatory Submissions
At Wealthy Technology, we simplify the creation and management of ICH CTD (Common Technical Document) submissions through intelligent automation. Our platform automatically structures and validates documentation across Modules 2–5, ensuring consistency, compliance, and faster review cycles.
By leveraging AI-powered document generation and smart validation tools, teams can focus on data quality and scientific integrity—while our system handles formatting, versioning, and global regulatory alignment.
Our solution minimizes manual effort, reduces submission errors, and accelerates approval timelines. It adapts to regional regulatory requirements, keeping documentation always audit-ready. With Wealthy, your CTD process becomes faster, smarter, and fully compliant.
Medical Device Compliance MDR & IVDR Submissions
Wealthy Technology empowers medical device manufacturers to achieve seamless compliance with MDR and IVDR regulations through intelligent automation. Our platform centralizes documentation, manages technical files, and ensures every component meets evolving European and global standards.
From risk management reports to clinical evaluations and post-market surveillance, our AI tools streamline every step, reducing time and manual errors.
With built-in validation and real-time compliance tracking, you can maintain transparency, ensure audit readiness, and bring products to market faster. Wealthy turns complex regulatory demands into clear, automated workflows.