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  Online Course  DIA 
Medical Communications eLearning Program 1-Jan  31-Dec  Online  Online Course  DIA 
Drug Safety eLearning Program 1-Jan  31-Dec  Online  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  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  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
Overview of Global Regulatory Affairs  24-Sept 2018 18-Nov 2018  Online  15  University Course  UC Irvine, Division of Continuing Eudcation 

January - March

January

Title Start Date End Date Location RAC Credits Type Company Name
FDA Enforcement in 2018-2019: Reading the Tea Leaves 24-Jan  24-Jan  Online  Webinar  Medmarc 

February

Title Start Date End Date Location RAC Credits Type Company Name
The "New CE Marking" for Medical Devices 9-Feb 9-Feb Costa Mesa, CA 6 Face-to-Face MDSS GmbH
The "New CE Marking" for Medical Devices 12-Feb 12-Feb Redwood City, CA 6 Face-to-Face MDSS GmbH
510(K) Submissions Workshop 26-Feb 27-Feb Irvine, CA 12 Face-to-Face Advanced Medical Technology Association
IDE Submissions Workshop 28-Feb 28-Feb Irvine, CA 6 Face-to-Face Advanced Medical Technology Association

March

Title Start Date End Date Location RAC Credits Type Company Name
The CMS Hospital Conditions of Participation (CoPs) Made Easy 2018 1-Mar  2-Mar  Online  10.5  Face to face  Compliance Online 
PMA Submissions Workshop 1-Mar  2-Mar  Irvine, CA, USA 12  Face to Face  Advanced Medical Technology 
An introduction to Veterinary Pharmacology 8-Mar  9-Mar  Online  12  Face to Face  Compliance Online 
The A to Z's of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals, Biologics, Medical Devices, Cosmetics, and Personal Care Products 8-Mar  9-Mar  Online  12  Face to Face  Compliance Online 
Labelling and Presentation of Food Products in the European Union 8-Mar  9-Mar  Online  11.5  Face to Face  Compliance Online 
FDA Forum 12-Mar  13-Mar  Palo Alto, CA, USA  12 Face to Face  Medical Device Manufacturers Association (MDMA)
Change Control Best Practices - Avoiding Unintended Consequences of Changes 15-Mar  16-Mar  Online  12  Face to Face  Compliance Online 
SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations 15-Mar  16-Mar  Online  12  Face to Face  Compliance Online 
FDA's New Import Program for 2018 - Strict Precision 15-Mar  16-Mar  Online  12  Face to Face  Compliance Online 
Recordkeeping and Documentation in a GLP Laboratory (US FDA, US EPA and OSHA Focus) 15-Mar  16-Mar  Online  12  Face to Face  Compliance Online 
Unannounced FDA Inspections 2017-2018: Navigating Cultural Differences 15-Mar  16-Mar  Online  12  Face to Face  Compliance Online 
Asia Pacific Device Summit 19-Mar  20-Mar  Yorba Linda, CA, USA 11 Face to Face  Brandwood Biomedical Pty Ltd
Risk Management in Medical Devices Industry 19-Mar  20-Mar  Online  12  Face to Face  Compliance Online 
FDA's Medical Device Software Regulation Strategy 20-Mar  21-Mar  Online  12  Face to Face  Compliance Online 
Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs) 22-Mar  23-Mar  Online  12  Face to Face  Compliance Online 
CLIA Waiver and Dual 510(k) CLIA Waiver Submissions to FDA 22-Mar  23-Mar  Online  12  Face to Face  Compliance Online 
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices 22-Mar  23-Mar  Online  12  Face to Face  Compliance Online 
Method Development and Validation for Assays Supporting Testing of Biologics 22-Mar  23-Mar  Online  12  Face to Face  Compliance Online 
FDA's New Import Program for 2018 - Strict Precision 22-Mar  23-Mar Online  12  Face to Face  Compliance Online 
ACH Risk Management 22-Mar  23-Mar  Online  12  Face to Face  Compliance Online 
Supplier Management for Medical Device Manufacturers 29-Mar  30-Mar  Online  12  Face to Face  Compliance Online 
Quality Control Laboratory Compliance - cGMPs and GLPs 29-Mar  30-Mar  Online  10.5  Face to Face  Compliance Online 

April-June

April

Title Start Date End Date Location RAC Credits Type Company Name
HIPAA Security and Breach Rule Compliance- Understanding Risk Analysis, Policies and Procedures and Managing Incidents 5-April  6-April  Online  10  Face to Face  Compliance Online 
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation) 9-April  10-April  Online  12  Face to Face  Compliance Online 
FDA Advisory Committee Master Class 26-April  27-April  Washington, DC, USA  12  Face to Face  CBI, a division of UBM Americas 

May

Title Start Date End Date Location RAC Credits Type Company Name
FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials 3-May  4-May  Online  12  Face to Face  Compliance Online 
The Veterinary Drug Approval Process and FDA Regulatory Oversight 17-May  18-May  Online  12  Face to Face  Compliance Online 
Bad Things Happen, But It Can Get Worse - Understanding FDA Post Market Regulations 23-May  25-May  Online  12  Face to Face  Compliance Online 
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada 21-May  1-June  Online  12  Face to Face  Compliance Online 

June

Title Start Date End Date Location RAC Credits Type Company Name
             
4th Annual ComplianceOnline Medical Device Summit 2018 7-June 8-May  Online  Face to Face  ComplianceOnline 
Introduction to Antimicrobials in Veterinary Medicine 21-June  22-June  Online  12  Face to Face  Compliance Online 
FDA's New Import Program for 2018 - Strict Precision 28-June  29-June  Online  12  Face to Face  Compliance Online