Corlytics helps your firm optimise all stages of the regulatory lifecycle from a single location.

One of the most significant challenges faced by Health and Life Science companies is managing the regulatory process and impact it has across the business.  This challenge is compounded by global complexity and ever-changing regulatory requirements.  Managing regulatory impact successfully can make the difference to bringing products and devices to market quickly and safely.

Corlytics provides a single platform to assess and understand draft and final regulatory guidance and its impact on your business. Building an intelligent and dynamic repository of requirements, digitising ‘call for comments’ assessments and producing intelligent outputs to support the submission process. Corlytics also provides a platform enabling the business wide regulatory compliance lifecycle, from assessing new regulatory changes, reviewing a detailed breakdown of regulations, the changes to comply with these and monitor this picture on an ongoing basis.

Corlytics has the ability to connect each element of the regulatory lifecycle on an easy-to-use platform, simplifying the submissions process by providing essential information in a single location. Our connectivity across your existing systems ensures that all stages of the regulatory lifecycle are optimised. This ensures compliance becomes an enabler for growth in your business and not a blocker or burden.