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Explore our library of blogs, insights, research papers, and more information on compliance in the life sciences industry.

Monitoring is the ongoing evaluation of business activity taking place, working as intended, and expected outcomes occurring. If your current compliance monitoring program does not align with this definition, it’s better to reevaluate the program to ensure it aligns. Other than ensuring a high level of comfort, a well-designed compliance monitoring program provides highly valuable […]

Compliance programs are constantly being enhanced by companies in response to the heightened compliance demands of the government along with a variety of other drivers, i.e., settlement requirements and industry standards – Compliance monitoring happens to be the one way through which companies can efficiently and effectively upgrade their compliance program and achieve success in […]

Meeting the federal and state aggregate spend reporting requirements demands significant time, resources, focus, and strategic processes from a life science organization. The evolving nature of the requirements and expectations set by the CMS make it extremely difficult for life science companies to comply with them, let alone monitor and stay updated with changes to […]

New policies, rules, and regulations followed by the dynamic nature of the life sciences industry make it much more overwhelming for compliance teams and companies to keep up with the evolving and heightened compliance demands, especially when you’ve chosen the wrong compliance partner to help you stay ahead of the game. Being considered one of […]

Mitigating compliance risks is important for life science companies. However, the pain of executing, measuring, and improving the effectiveness of a compliance program is well-known within the life science industry and by compliance teams. The highly scrutinized nature of the life science industry demands certain laws and regulations to be followed to avoid penalties and […]

A compliance program is an internal system or process composed of a set of rules, regulations, and guidelines created to enable life sciences to maintain legal, ethical, and professional operational standards while reducing the risk of breaching rules and regulations within the industry by following the laws issued by the Health & Human Services (HHS) […]