ReadyTech Consulting partners with MedQAIR

Integrated Legal, Compliance, and Regulatory Expertise for MedTech

ReadyTech Consulting is proud to partner with MedQAIR, a specialized consultancy focused on quality, compliance, and regulatory support for medical devices, digital health, and AI-driven technologies.

While MedQAIR ensures alignment with EU MDR, IVDR, FDA, ISO 13485, ISO27001, and AI Act requirements from concept to commercialization, ReadyTech Consulting complements this with fractional in-house legal support, contract management, certifications management, GDPR compliance, and cross-border legal expertise. Together, we help MedTech companies navigate both the technical regulatory pathway and the legal framework needed to scale globally.

Why This Partnership Matters

Full Spectrum Support

Our combined expertise covers the full lifecycle:

• MedQAIR: Regulatory strategy, QMS design and implementation, risk management, MDR/IVDR compliance, post-market surveillance.
• ReadyTech Consulting: Legal advisory, certification management, data protection and privacy governance, contract management, cross-border compliance.

Audit Readiness

We collaborate closely with MedQAIR’s team of medical device and regulatory experts – aligning their deep expertise in compliance, quality systems, and technical requirements with our legal, governance, and data protection capabilities. This partnership ensures that clients benefit from a coordinated approach that addresses both the regulatory and operational dimensions of success, reducing risk, accelerating timelines, and supporting audit readiness.

From Startup to Global Scale

Whether launching your first SaMD or managing complex multi-country operations, our partnership adapts to your stage, offering flexible, business-aligned expertise to support sustainable growth and international market entry.

Learn more about our new partners on their official website here.