Welcome to our new website! If this is the first time you are logging in on the new site, you will need to reset your password. Please contact us at firstname.lastname@example.org if you need assistance.
Your membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
This comprehensive resource covers product change evaluation, postmarket surveillance, audit/inspection compliance, and various other laws and regulations pertaining to maintaining a product on the market.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
Are you planning to take the RAC-Drugs exam in 2023?
Join others from the regulatory community for a workshop/study group crafted to sharpen your critical, analytical and strategic test-taking skills. The sessions will be facilitated by a panel of certified (RAC) regulatory professionals that are subject matter experts in their field.
During the workshop, faculty will review challenge questions similar to the style and content of the RAC Exam. This style of teaching has been used in other preparatory workshops and has been determined to be most useful for those taking the RAC Exam.
Participation in this workshop should not be your only method of exam preparation. RAPS provides many exam preparation materials which can help you develop a comprehensive study plan.
NOTE: Registration for the Summer 2023 RAC Window closes on 15 June, 2023. The Spring testing window runs from 10 July- 18 August 2023.
Regular: $495 Member | $580 Nonmember
Attendees will learn how to analyze around 200 RAC Drug questions and how to pick answers that look to have two correct answers.
This workshop is recommended for regulatory affairs professionals with:
The two-day program will break down questions from RAC Drugs Practice Exams, focusing first on the US, moving on to EU and ending with Global. The course will be open discussion with questions and the amount of time on the topics will be dictated by the attendees. There will be a study group on RAPS regulatory exchange where you will be able to further discuss questions and study strategies with the presenters and fellow attendees
The program will run from Wednesday, 31 May 2023 11:00 AM- 4:00 PM ET through Thursday, 1 June 2023 from 11:00 - 4:00 PM EST
Tyler VandivortAmplicore Inc
Tyler Vandivort, PhD, RAC is a toxicologist by training whose graduate/postdoctoral work as an NIH Training Grant recipient at the University of Washington and Cedars-Sinai Medical Center focused on the role of extracellular matrix proteins in the acute and chronic immune response to sterile and non-sterile injury. During his more than 5 years of contract research organization (CRO) experience, first as an Immunotoxicology Research Scientist at Charles River Laboratories, and then as a consultant in the Regulatory Affairs and Scientific & Strategic Development group at Medpace, Tyler has cultivated an understanding of the key procedural and strategic components of nonclinical and early phase clinical development that drive program success. He received a Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professionals Society (RAPS) in 2019.
Sanje GoonasekeraAmplicore Inc
Regulatory Affairs at Magenta Therapeutics
Dr. Sanje Goonasekera is an Associate Director of Regulatory Affairs at Magenta Therapeutics, a company developing medicines to bring the curative power of immune system reset through stem cell transplant to more patients with blood cancers, genetic diseases and autoimmune diseases. He also serves as an adjunct professor at the James L. Winkle College of Pharmacy at the University of Cincinnati. He has more than 10 years of experience in pre-clinical and clinical research. Prior to Magenta, Dr. Goonasekera was at Medpace, a clinical research organization conducting global clinical research for the development of drugs and medical devices. He holds both the RAC Drugs and RAC US certifications.
Dr. Darin S. OppenheimerAmplicore Inc
Senior Director, US Regulatory Diabetes Group Medtronic
Darin joined Medtronic with 19 years of experience in many facets of the product development lifecycle, including regulatory submissions and due diligence. He has actively participated with industry trade organizations and on standards committees. His time as a research and development scientist focused on pharmaceuticals and medical device diagnostic applications for biomarker and drug discovery.
All cancellation requests must be submitted in writing to email@example.com. Cancellations will receive a full refund minus a 20% administrative fee. RAPS is unable to accept cancellations by phone.
Paid registration substitutions may be accepted with written approval from RAPS for requests received before the start of the event. To transfer a registration, email firstname.lastname@example.org with the event title, name of the original registrant and the contact information for the new attendee.
For additional hands-on support, you can also connect with RAPS support 30 min prior to the workshop: https://www.raps.org/website/virtual-event-helpFor account support, contact the RAPS Support Center: +1 301 770 2920, ext. 200 (8:30 am–5:30 pm EST, Monday–Friday) or email email@example.com.