Building the case that regulators expect and science demands
Regulatory Evidence Preparation
Organizations introducing or modifying regulated products, services, processes, or data practices must not only generate strong evidence, but also present it in formats and narratives that align with jurisdictional norms and regulatory expectations.
How RSI delivers Regulatory Evidence Preparation
RSI will conduct assessments in line with regulatory guidelines and produce robust reports and evidence summaries that meet regulatory requirements for submission. We use quality assurance practices to provide clarity, consistency, and defensibility. The team aligns technical content with regulatory frameworks and communication norms—supporting smooth, credible engagement with oversight bodies.
Why RSI is trusted to deliver
The RSI team has decades of experience working with government and private sector clients to produce reports in line with requirements from numerous regulatory agencies, including the United States Environmental Protection Agency and the Food and Drug Administration, Health Canada, Environment and Climate Change Canada, and Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) in the European Union.
Why this image?
The “APPROVED” stamp symbolizes the end goal of regulatory evidence preparation: meeting rigorous standards with clarity, credibility, and completeness. While the stamp itself is simple, it stands on a foundation of well-organized data, sound analysis, and defensible documentation. This image highlights the pivotal role that high-quality evidence plays in enabling regulators to make confident, timely, and legally sound decisions.