Stronger decision-making through collaboration

Indivior is a global speciality pharmaceutical enterprise with nearly 1,000 employees and revenues exceeding £1 billion. It researches and makes pharmaceutical products which help patients with diseases of addiction.

Maria Sanderson, Indivior’s EHS Manager, began looking for an electronic quality management system in 2016 to update and improve how the company planned, managed and reported on its corrective and preventive action (CAPA). Indivior is regulated by bodies such as the FDA and MHRA, and so needs to demonstrate that its operations meet the very highest standards.

Indivior chose Qualsys’s GRC software for its advanced audit trail functionality, which enables the company to control change, issues and actions through to completion. And the system’s dashboard and custom reports allow Indivior to interpret large volumes of data which it can then use in its decision-making.

indivior medical

You may also be interested in

ISO 13485
Hundreds of companies use Qualsys's software to plan and manage a medical device quality management system which meets ISO 13485 best practices. Find out why we're the UK's highest rated solution provider.
Read more
ISO 14971
ISO 14971 defines international requirements for risk management systems for medical devices. Our software helps you to implement best practices throughout the entire lifecycle of your medical device.
Read more
Medical device quality management software
Protecting your patients and getting your medical devices to market starts with a strong quality and compliance management system. Our software and services guide you through the entire process, ensuring you have a best-practice system which meets the most rigorous compliance requirements.
Read more
Global pharmaceutical businesses, NHS trusts and other life science businesses have validated iterations of EQMS as compliant with the requirements of regulations such as GAMP 5, ISO 9001, ICH GCP E6 and FDA 21CFR Part 11, and electronic signature legislation such as the EU Electronic Signatures Dir...
Read more