The Regulatory Compliance Certification (RCC) is the industry standard for validating specialized regulatory expertise. Specifically, the RCC-MDR and RCC-IVDR are professional certifications — not training courses — that objectively confirm your proven knowledge and relevance. To earn the credential, you must meet eligibility criteria, pass a comprehensive exam, and maintain currency via ongoing professional development.
Why is the RCC necessary?
EU MDR and EU IVDR regulations mandate that manufacturers designate a Person Responsible for Regulatory Compliance (PRRC). Organizations worldwide urgently require qualified professionals with current, verified expertise for this mission-critical role.
The RCC addresses this need by providing objective, third-party evidence of your deep expertise, including at least four years of directly-related regulatory experience (or equivalent).
- For Experienced Professionals: it proves your deep expertise is current.
- For All Candidates: it cements your authority and provides verifiable evidence of conformity to regulatory requirements, helping to reduce organizational risk and making you a highly attractive job candidate or incumbent.
Why choose the RCC?
The RCC is the only professional certification specifically designed to validate expertise in EU MDR (RCC-MDR) or IVDR (RCC-IVDR). It is recognized as the industry standard for confirming you:
- Possess the specialized knowledge.
- Have been tested on that knowledge.
- Are committed to keeping your expertise up to date.
Why attend this webinar?
Join RAPS for this free, essential session to learn how earning an RCC certification can significantly bolster your qualifications to meet industry requirements as a trusted, verified PRRC professional.
Registration Fees & Deadlines
Free
Learning Objectives
You will leave this session prepared to:
- Verify Your Eligibility: Understand the experience requirements needed to qualify.
- Assess Your Readiness: Determine if the RCC program is right for you and your career.
- Develop Your Action Plan: Develop an action plan that includes exclusive sample exam questions and detailed lists of exam topics.
Who Should Attend?
The new RCC credentials are intended for individuals who need or want to demonstrate that they are compliance professionals who are knowledgeable in EU Medical Device (MDR) or In Vitro Diagnostics (IVDR) regulations. Four years of related experience or the equivalent is required to sit for the exam.
Audience Learning Level
Basic: Content is introductory in nature and requires no requisite knowledge or experience to grasp concepts and related exercises. Basic educational activities are meant to establish a foundation of knowledge and/or competence that will be expanded upon in practice or in higher level activities.
Speakers
To Be Determined
Questions
Contact the RAPS Support Center:
Call +1 301 770 2920, ext. 200 (8:30 am–5:30 pm EST, Monday–Friday) or email
support@raps.org.