RQM+ Acquires Giotto Compliance

RQM+, the world’s leading MedTech service provider, today announced the acquisition of Giotto Compliance from Giotto Compliance is a global, all-in-one artificial intelligence (AI) platform designed to increase the efficiency and effectiveness of regulatory reports and filings across the product development lifecycle for medical device and in vitro diagnostics manufacturers.

“We have only begun to scratch the surface of what can be achieved by integrating Giotto Compliance AI technology throughout our consulting, clinical trials, laboratory and reimbursement services,” said RQM+ CEO Margaret Keegan. “We are fortunate to have our Chief Digital and Technology Officer Alaric Jackson lead this new business unit. He will expand the capabilities of Giotto Compliance to enhance our current services as well as offer a standalone solution that can be leveraged to streamline regulatory document development while maintaining compliance with global regulations.”

Giotto Compliance will operate as an independent RQM+ business unit and serve its growing customer base. The business will be led by Jackson, who has more than 20 years of technology leadership experience within the contract research organization (CRO) and pharmaceutical industries. In previous roles, he automated and streamlined regulatory solutions to enhance compliance, productivity and quality using advanced technologies and digital workflows.

“We are excited to offer the MedTech industry a step change using cutting-edge AI that improves quality while increasing speed-to-market,” said Jackson. “Currently, Giotto Compliance reduces the burden of data collection, analysis and creation of regulatory documentation, such as clinical evaluation reports, allowing our team to focus on creative solutions, complex problem solving and impactful work. We will accelerate the creation of AI models and functionality to expand its capabilities across a wide range of processes for MedTech manufacturers, regulators and service providers.”

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