By: Priyanka Sharma, Senior Vice President, Software Engineering, Suvoda LLC
Snapshot:
- Continuous safeguarding: effective risk management includes regular assessment and adaptation as technology and regulations evolve.
- Proactive risk management: clinical trials require risk analysis tailored to each organization's unique tolerance level.
- Privacy balance: organizations must protect patient data while advancing research by engaging patients transparently throughout a trial about risks and benefits.
In clinical trial settings, advancing innovation while upholding regulatory compliance and minimizing risk is an ongoing responsibility. As formal regulations, informal guidance, and industry best practices continue to evolve, what are some of the considerations organizations can keep in mind when navigating this landscape?
Innovation with integrity matters
New technologies can enhance patient experiences, increase site and sponsor operational efficiency, and improve data quality. But their success can depend on thoughtful implementation—balancing safety, risk, and compliance alongside progress. Clinical trials have inherent and complex risks to manage, such as patient privacy or safety (e.g. ensuring patients receive the correct drug and dose at the right time); trial integrity (e.g. proper randomization or maintaining the study blind); regulatory compliance (e.g. clear audit trails or restricted user access); and secure system operations (e.g. functionality that enforces study protocols.)
The clinical trial industry can benefit when companies deploy innovative technologies with careful attention to these risk factors. Solutions that include robust security from the earliest design stages help maintain compliance without hampering progress. When regulations are viewed not as barriers but as guardrails—they can guide safe, effective innovation that supports medical research and hopefully can improve lives.
Understanding the evolving regulatory landscape
The clinical trial industry operates within a robust regulatory environment that includes both clearly defined rules and areas open to interpretation. During a recent webinar, “Applying Technology Advancements to Overcome Challenges in Clinical Trials,” we discussed how a clear understanding of regulatory compliance and privacy requirements has become a baseline expectation of vendors in our industry.
A challenge arises when teams must decide how much weight to assign to guidance that hasn’t yet become formal regulation. The answer often depends on an organization’s size, risk appetite, and strategic goals. There’s no one correct way to assess and manage risk in clinical trials. What matters most is that organizations conduct thorough, context-specific risk analyses—always with patient safety at the center.
Bringing safety and innovation together
As clinical trials embrace new technologies, protective frameworks must evolve in parallel. When thoughtfully designed, these frameworks can allow innovation to enhance—not compromise—trial integrity.
“There are quite a few factors in our industry specifically, which are essential for adoption of technology in a risk-averse manner,” I shared during the webinar.
These include:
- Risk analysis: start by assessing how new technology might impact patient safety and data integrity—and put proactive plans in place to address those risks.
- Operational controls: the basics matter. Clear Standard Operating Procedures (SOPs) and regular staff training help teams follow proper procedures when using new tools.
- Incident response plans: well-defined processes help trial teams react effectively if unexpected problems occur.
- Technical safeguards: secure systems—with features like audit trails, encryption, and GDPR compliance (General Data Protection Regulation in the European Union)—form the backbone of trustworthy digital trials.
Empower patients through transparent data use
In addition to safety, patient data privacy in clinical trials is another important component of risk management. From the very beginning of a trial, patients, who are at the heart of clinical trials, must consent to sharing their data with researchers. While patient information must be protected, many participants are willing to share personal data when they understand its purpose and value. Transparency builds trust. When patients know how their data will be used and what protections are in place, they can make more informed, confident choices about their participation. This balance between protection and progress echoes the broader balance needed in our approach to innovation itself.
Treat innovation like a muscle—it requires regular exercise
Rather than viewing innovation as a series of dramatic breakthroughs, I see it as steady, intentional refinement, incorporating risk management and compliance all along the way. During the webinar, I shared that “my vision of innovation is continuous iteration. Innovation tends to be a muscle which you keep on exercising to ensure that you reach your outcomes.”
With this mindset, organizations can stop waiting for revolutionary changes, and instead focus on meaningful, incremental improvements—guided by real-world user feedback, evolving regulatory guidance, and updated risk management. The most effective innovations often emerge not from sudden inspiration but from careful observation of what works (and what doesn't) in practice.
Careful balance of risk, regulation, and innovation: an ongoing priority
Risk management isn’t a one-time box to check—it’s a continuous process. As I said during the webinar, “This is not a magic bullet. It needs to continue to evolve with the technology innovations happening in the industry and the changing landscape we see.”
This aligns with the industry’s shift toward adaptive trial designs and continuous oversight. Just as trials now incorporate more flexibility, our approaches to risk must evolve as well—staying aligned with new tools, patient needs, and regulatory updates.
Innovation in clinical trials isn’t just about adopting new tools—it’s about doing so thoughtfully, with patient safety, and regulatory integrity in mind. By embracing an intentional, transparent approach, companies can drive meaningful progress while earning the trust of patients, sites, and regulators.
Author
Priyanka Sharma
Senior Vice President, Software Engineering,
Suvoda
ON-DEMAND WEBINAR
Applying technology advancements to overcome challenges in clinical trials