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Innovation and compliance
Infomed has partnered with biotech, medical devices organisations, financial institutions, and regulatory agencies to create innovative systems and bring groundbreaking products to market.
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We offer a fully customisable, end-to-end suite of services, and we empower our clients to overcome regulatory complexities and support with their market readiness.
FDA 🟠GMPðŸŸ
SAHPRA🟠EU MDR
🟠ISO 13485
FDA🟠GMP🟠SAHPRA🟠EU MDR🟠ISO 13485
SAHPRA🟠EU MDR
Explore Our Core Services
Our experts understand what it takes to get products to market and help design efficient and compliant systems as needed to help you meet your goals.
Ensure your compliance with Infomed's team of experts
Talk to our team of experts to see how Infomed can propel your business into new markets.
Four Simple Steps:
Initial Consultation
Connect with one of our experts to discuss your specific regulatory needs and challenges. This is where we listen and understand your goals.
Receive a Proposal
We will provide a comprehensive proposal and a transparent, non-binding quote tailored to your projject scope and objectives.
Project Kick-Off
Finalize our agreement following the proposal approval. We officially begin our work and guide you towards your goals and objectives.
Execution and Delivery
We execute on the agreed-upon deliverables, and produce high-quality results. Final payment i ssubmitted upon your work satisfaction.