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The regulatory function is vital in making safe and effective healthcare products available worldwide. Individuals who ensure regulatory compliance and prepare submissions, as well as those whose main job function is clinical affairs or quality assurance are all considered regulatory professionals.
One of our most valuable contributions to the profession is the Regulatory Code of Ethics. The Code of Ethics provides regulatory professionals with core values that hold them to the highest standards of professional conduct.
Your membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
Like all professions, regulatory is based on a shared set of competencies. The Regulatory Competency Framework describes the essential elements of what is required of regulatory professionals at four major career and professional levels.
Join the brightest minds in regulatory at the annual Regulatory Convergence. See the global regulatory community in action. Intensive workshops. Topical sessions. Meet ups with regulators. This is where it all comes together.
With so many global regulation changes, staying informed is a challenge. Join other regulatory professionals as you navigate the gray together.
For 20 years, our flagship publication, Fundamentals of US Regulatory Affairs, has been giving regulatory professionals the insights and answers they need, right at their fingertips.
There are hundreds of RAC testing centers available worldwide. Either RAC exam (Devices and Drugs) may be taken at any location. Find an upcoming exam at a location near you.
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Students: $20RAPS Member: $30Nonmember: $40
*Fax/email in a completed registration form to get the student rate.
Pharmaceutical companies often encounter challenging privacy issues when determining what clinical trial information to disclose and communicating research results. How can these companies appropriately balance privacy concerns with transparency? Join us for an in-depth conversation about navigating privacy regulations, including GDPR and HIPAA, when disclosing clinical trial data and results. There also will be a discussion on promoting clinical research transparency. The levels of transparency that will be covered include:
This event, hosted by the University of the Sciences, is brought to you by the RAPS Philadelphia Chapter to encourage knowledge sharing and community development. A light meal will be provided for all attendees, and RAC holders may claim two RAC recertification credits.
Featured speaker:Darshan Kulkarni, PharmD, MS, Esq., The Kulkarni Law Firm
Local contact: Fredy Varela, RAC, MRA, RAPS Philadelphia Chapter
RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation.
Photo Release: By registering for this program, you acknowledge that your picture may be taken by RAPS agents and consent to the use of your name and likeness by RAPS for any RAPS use as deemed appropriate by the organization.
Cancellation Policy: Registration fees for this event are nonrefundable. Substitutions may be accepted with written approval from RAPS. If you have questions or concerns, please contact RAPS customer service at +1 301 770 2920, ext. 200, or via email at support@raps.org.