Posted on Regulatory Compliance. 18 May, 2021
Major research institutions and academic centers operate in an increasingly complex global network of scientific collaborators. In recent years, there has been a rising number of partnerships between non-profit research institutes and pharma, driven by cuts to academic research budgets, waning pipelines, and the pharma industry’s emphasis on open innovation. This can make regulatory compliance that much more difficult.
Despite the rise in number of collaborations, there are a number of challenges pharma and academia face when establishing their alliances, in particular aligning on opposing goals. For pharma, these partnerships are about gaining access targets, molecules, and academic investigators that can help get cures to the clinic. Academia is driven by the “publish or perish” culture – which can also cause some IP concerns for pharma. Similarly, rather than focusing solely on the clinic as the end goal for a molecule, academia’s efforts are often directed toward determining how and why a drug did or didn’t work. These often-cited challenges, though significant, do not tell the whole story.
Research regulatory compliance is emerging as a major factor in public-private collaborations. To win major partnerships and sustain operations in an increasingly competitive research funding environment, research compliance must be on your list of organizational priorities. No longer an insular activity, research in a complex partner ecosystem with increasingly complex regulations requires serious on-going attention, whether from an outside party or internal compliance function or both. From data management to animal use and the requirements surrounding human subjects, assessing your compliance risk even in exploratory research environments is no longer a nice-to-have. Unfortunately, many traditional academic centers face a lack of institutional infrastructure and resource to deal with compliance.
The research administration environment grows increasingly complex with changing regulations, inconsistencies among agencies, lack of information (meaningful and timely reports), thus generating more risk than institutions recognize. There remains a vast disconnect between the award environment, (during which the funding agency and the PI focus primarily on the research itself) the degree of flexibility that is perceived to exist while the research is being conducted, and the audit environment that follows. The current environment often places increased emphasis on accountability during a time when many institutions are faced with significant financial pressures and mandates to reduce staff. Numerous research institutions have indicated that compliance costs have grown during the past decade. More telling than the increases in associated research compliance costs are trends showing that these costs have increased more rapidly than the associated direct research expenditures, such as salaries, lab supplies, and research equipment.
Research compliance impacts:
In addition to increasingly complex regulations, the trend towards moving on-premise systems to cloud-based or hybrid environments adds further complications to the research compliance landscape. While the move to the cloud contributes to organizational agility and efficiencies, cloud-based environments must be validated appropriately and are often managed differently from traditional on-premise solutions.
So, how do research institutions get a handle on the issues? To start, let’s identify the current areas of compliance that should be addressed. This widespread, yet non-exhaustive, list of regulatory compliance issues creates a complex charge for the research compliance program at an institution.
How do I Design a Comprehensive Compliance Program?
Before designing a program to address research compliance in your organization, you must first have a deep understanding of your processes, data management practices, infrastructure and IT systems that are impacted. The first step and best practice is always to start with a thorough analysis of the current state, including in-scope business processes, systems, and procedures (such as current data management practices) to ensure quality compliance with governing regulations. This can be performed by an internal audit or oversight function or pursued with an external third-party with the appropriate experience in system and process auditing, regulatory and compliance, risk management processes, laboratory informatics systems, and organizational quality management practices.
Once you have performed the analysis, turn your attention to developing a comprehensive compliance program designed to get you to where you want to be over time. The following eight elements are considered as necessary for a comprehensive compliance program.
Implementing the plan is time consuming and requires buy in across the organization, dedicated resources with defined roles, and enforcement mechanisms. In general, a proactive approach to creating a compliance program will allow an institution to manage its compliance risk without imposing unnecessary constraints on the institution’s operations. Strong compliance programs not only benefit research institutions by reducing the risk of significant non-compliance but also tend to increase accountability, clarity, and information flow across the enterprise.
Astrix has been an industry leader for over 25 years in helping scientific organizations implement and integrate improved informatics systems in the laboratory. Our experienced team of expert informatics consultants bring together technical, strategic, regulatory and content knowledge to provide the most effective solutions to problems faced by scientific organizations. Our domain experts have helped hundreds of companies globally effectively navigate their digital transformation journey.
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