Compliance Tracking
It's challenging to ensure compliance across today's complex regulatory landscape
Does the compliance process feel overwhelming?
Implementing compliance best practices is critical to your business. Not only do you need to
meet requirements coming from government organizations, but your customers and suppliers
may also have their own compliance requests.
If you’re not using solid and rigorous processes to electronically track controls and documents, you
may feel like you’re drowning in spreadsheets and three-ring binders crammed with paper, making
the compliance process feel overwhelming.
And you may worry because failure to comply comes with added risk to patient safety, not to
mention a significant financial impact on your organization.
Be confident in your compliance tracking
Merit for Life Science is designed with compliance tracking integrated at all levels. You have the comfort
of knowing you’re ready with fully transparent and rigorous compliance necessary for your biotech,
pharma, or medical device organization.
Measuring compliance is critical, but in manufacturing, compliance alone is not enough. Merit for Life
Science provides a comprehensive platform to establish and maintain a culture of quality while also
supporting regulatory compliance, allowing you to continuously improve the quality of your operations
and your products.
Compliance Tracking
Ensure that as electronic signatures are collected and managed, records associated with those electronic signatures are fully Health Canada and CFIA compliant.
Leverage audit trails that are readily accessible directly with the record and understandable using common business language.
Prove to leadership and outside parties that you follow standard operating procedures with an easy-to-use and understand audit tracking system that puts audit details at your fingertips.
Inspire confidence with Canada Health inspectors using this extensible digital framework by HSO, Microsoft, and Merit's that simplifies your compliance processes.
Validate your system with the confidence that you can maintain it with a consistent schedule and IV&V automated tools for repeatable validation.