Category: HCP Engagement

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

5 Ways to Meet Aggregate Spend Reporting Deadlines

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 […]

The Vital Role of Compliance Partnerships in Life Sciences

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 […]

4 Steps to Enhancing the Effectiveness of a Compliance Program

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 […]

5 Essential HHS Laws for Life Sciences Companies

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) […]

Navigating Compliance Challenges in Life Sciences: Strategies and Solutions

Compliance requirements can be difficult to abide by, but a strategic process consisting of the identification of risks, analysis, and remediation can play an essential role in enabling drug and device manufacturers to develop effective compliance programs. But before diving directly into the development phase, first and foremost comes the necessity of understanding the totality […]

Reimagining Compliance Modernization in the Life Sciences Industry

A modernized approach, one that involves the utilization of data analytics, technologies, and automation, to compliance, is the way forward for life sciences companies. Being a broad mandate, compliance modernization spans how the function is governed and covers various other tangents, i.e., technologies, tools, analytics, and their uses. Hence, several parts of a business get […]