RAPS offers a range of certifications designed to assess and validate expertise in regulatory affairs, primarily in healthcare and life sciences sectors. These certifications typically cover a broad array of topics, including regulatory compliance, global regulatory systems, clinical trials, product lifecycle management, and risk management. Candidates are expected to demonstrate in-depth knowledge of regulatory frameworks, guidelines, and standards, often requiring familiarity with industry-specific regulations and international laws. RAPS certifications support various career paths in regulatory affairs, including roles in regulatory policy, submission management, and compliance, with professionals often working in pharmaceutical, biotechnology, and medical device industries.