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As the central resource for regulatory professionals worldwide, RAPS is committed to helping you succeed at every stage of your career.

The Industry Events listing is an interactive online resource that showcases non-RAPS professional development opportunities. It is designed to expand your exposure beyond RAPS' offerings and connect you to a diverse range of relevant programs in regulatory, science, business and related fields.

Throughout the Year

Title Start Date  End Date Location RAC Credits Type Company Name
Drug Development and Life Cycle Management eLearning Modules 1-Jan 31-Dec  Online  6  Online Course  DIA 
Medical Communications eLearning Program 1-Jan  31-Dec  Online  6  Online Course  DIA 
Drug Safety eLearning Program 1-Jan  31-Dec  Online  6  Online Course  DIA 
Clinical Trial Fundamentals eLearning Program 1-Jan  31-Dec  Online  7.5  Online Course  DIA 
Regulatory Writing Overview: Roles, Documents, and Process 1 May 2017  30 April 2018  Online  3  Online Course  American Medical Writers Association 
Effective Project Management: Paving the Path to Successful Regulatory Documents 1 June 2017  31 May 2018  Online  12  Online Course  American Medical Writers Association 
Clinical Study Report Development and the Investigator’s Brochure 1 June  31 May 2018  Online  12  Online Course  American Medical Writers Association 
Drug Safety and Pharmacovigilance - PHRMSCI X493 26 June 2017  3 Sept 2017 Online  15  Online University Course  University of California, Irvine Division of Continuing Education 
Building a Technical File for Global markets 14-Nov 2017  14-Nov 2018  Online  1  Webinar  Brandwood Biomedical 
Documents & Dialogues of Drug Dev & Registration 19- Jan 2018  11-May 2018  West Lafayette, IN, USA  15  University Course  Purdue University 
Good Regulatory Practices 19-Jan 2018 11-May 2018  West Lafayette, IN, USA 15  University Course Purdue University 
Quality Culture 19-Jan 2018  11-May 2018  West Lafayette, IN, USA  15  University Course  Purdue University 
Regulatory Requirements for Medical Devices 8-Jan 2018  16-Dec 2018  Online  15  University Course  UC Irvine, Division of Continuing Education
Post-Approval Compliance Requirements for Pharmaceutical Products 8-Jan 2018  9-Sept 2018  Online  15  University Course  UC Irvine, Division of Continuing Education
Regulatory Requirements for Pharmaceutical Products 2-April 2018  16-Dec 2018  Online  15  University Course  UC Irvine, Division of Continuing Education
Medical Product Life-Cycle Management  2-April 2018  16-Dec 2018  Online  15  University Course  UC Irvine, Division of Continuing Education
Quality Management, Audits & Inspections 24-August 2018 8 December 2018 West Lafayette, IN 15 University Course Purdue University Polytechnic Institute
Overview of Global Regulatory Affairs  24-Sept 2018 18-Nov 2018  Online  15  University Course  UC Irvine, Division of Continuing Eudcation 

October-December

October

Title Start Date End Date Location RAC Credits Type Company Name
510(K) Submissions Workshop - Fall 2018 15-Oct 16-Oct Washington, DC 12 Face-to-Face Advanced Medical Technology Association
IDE Submissions Workshop - Fall 2018 17-Oct 17-Oct Washington, DC 6 Face-to-Face Advanced Medical Technology Association
PMA Submissions Workshop - Fall 2018 18-Oct 19-Oct Washington, DC 12 Face-to-Face Advanced Medical Technology Association

November

Title Start Date End Date Location RAC Credits Type Company Name
             
             

December

Title Start Date End Date Location RAC Credits Type Company Name
International MDR Happening - "The NEW CE MARKING" 11-Dec 12-Dec Hannover, Germany 12 Face to Face MDSS GmbH
             

January - March

January

Title Start Date End Date Location RAC Credits Type Company Name
             

February

Title Start Date End Date Location RAC Credits Type Company Name
             

March

Title Start Date End Date Location RAC Credits Type Company Name
2019 FDA Forum 14 - Mar 15 - Mar Palo Alto, CA 12 Face-to-Face MDMA Medical Device Manufacturers Association