Industry Events

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.

Interested in becoming a provider? Fill out our online provider registration form or contact Alyssa Blackwell at +1 410 584-1989.

  • Ongoing
  • 2017 Q1
  • 2017 Q2
  • 2017 Q3
  • 2017 Q4

Throughout the Year

TitleStart Date End DateLocationRAC CreditsTypeCompany Name
Regulatory Requirements for Pharmaceutical Products - EECS_X445.269 Jan 201719 March 2017 Online 15 Online University Course University of California, Irvine Division of Continuing Education 
Regulatory Affairs Planning and Management: Concept Review and Evaluation - BME_X4129 Jan 201719 March 2017 Online 15Online University CourseUniversity of California, Irvine Division of Continuing Education 
Overview of Global Regulatory Affairs - PHRMSCI_X4903 April 2017 11 June 2017 Online 15 Online University Course University of California, Irvine Division of Continuing Education
Drug Safety and Pharmacovigilance - PHRMSCI X49326 June 2017 3 Sept 2017Online 15 Online University Course University of California, Irvine Division of Continuing Education 

January-March

January

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
From Addiction to Zika: Current Issues in Public Health Law2-Jan 13-Jan Online 15 Online University Course Mitchell Hamline School of Law Health Law Institute 
Legal Compliance Essentials for Drug, Device, and Biotech Companies2-Jan 13-Jan Online 15 Online University Class Mitchell Hamline School of Law Health Law Institute 
Regulatory Requirements for Pharmaceutical Products - EECS_X445.269-Jan 19-March Online 15 Online University Course University of California, Irvine Division of Continuing Education
Regulatory Affairs Planning and Management: Concept Review and Evaluation - BME_X4129-Jan 19-March Online 15 Online University Course University of California, Irvine Division of Continuing Education 
Computerized Systems and Data Integrity – Avoiding The Top Five Regulatory Pitfalls12-Jan 12-Jan Online Webinar FutureCorp Consulting DBA Compliance Trainings 
Clinical Trials for The Intended Use of Software as a Medical Device17-Jan 17-Jan Online Webinar FutureCorp Consulting Inc DBA Compliance Trainings 
Brexit & the EEA QPPV – What Now?18-Jan 18-Jan Online Webinar Mapi Group 
Rare Diseases and Orphan Drugs in Latin America  21-Jan21-Jan GlobalWebinarMapi Group
FDA Scrutiny of Promotion and Advertising Practices24-Jan 25-Jan San Francisco, CA, USA 12 Face to Face ComplianceOnline 
FDA Outlook 2017 - An Overview of Changes for 201725-Jan 25-Jan Online Webinar Medmarc 
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions26-Jan 27-Jan Orlando, FL, USA 12 Face to Face ComplianceOnline 
Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)26-Jan 27-Jan San Francisco, CA, USA 12 Face to Face ComplianceOnline 
Supplier and Contractor Qualification and Control for Life Science Industry26-Jan 27-JanTampa, FL, USA 12 Face to Face ComplianceOnline 
Essentials Of USP Microbiology - Reading Between the Lines of the USP General and Information Microbiology Chapters31-Jan 1-Feb Orlando, FL, USA 12 Face to Face ComplianceOnline 

February

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials2-Feb 3-Feb San Diego, CA, USA 10 Face to Face ComplianceOnline 
Navigating the Maze for Post-Market Compliance -- Complaint Handling, MDRs, Recalls and Proposed Guidance on FDA Risk Benefits2-Feb 3-Feb Tampa, FL, USA Face to Face ComplianceOnline 
21 CFR Part 11 Compliance for SaaS/Cloud Applications3-Feb 3-Feb San Diego, CA, USA 12 Face to Face ComplianceOnline 
Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products2-Feb 3-Feb Tampa, FL, USA Face to Face ComplianceOnline 
Analytical Instrument Qualification and System Validation7-Feb 8-Feb San Francisco, CA, USA 12 Face to Face ComplianceOnline 
SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations9-Feb 10-Feb Scottsdale, AZ, USA 12 Face to Face ComplianceOnline 
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)9-Feb 10-Feb San Francisco, CA, USA 12 Face to Face ComplianceOnline 
FDA Recalls - Before You Start, and After You Finish9-Feb 10-Feb San Jose, CA, USA 12 Face to Face ComplianceOnline 
Understanding and Implementing a Quality by Design (QbD) Program9-Feb10-Feb Tampa, FL, USA 12 Face to Face ComplianceOnline 
Data Integrity: FDA/EU Requirements and Implementation13-Feb 14-Feb San Francisco, CA, USA 12 Face to Face ComplianceOnline 
FDA's Medical Device Software Regulation Strategy16-Feb 17-Feb San Francisco, CA, USA 12 Face to Face ComplianceOnline 
Effective Design, Validation and Routine Maintenance of Pharmaceutical Water16-Feb 17-Feb San Diego, CA, USA 12 Face to Face ComplianceOnline 
Designing and Sustaining New and Existing Product Stability Testing Program20-Feb 21-Feb Atlanta, GA, USA 12 Face to Face ComplianceOnline 
HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer23-Feb 24-Feb San Francisco, CA, USA 10Face to Face ComplianceOnline 
Effectively Addressing and Remediating FDA's Form 483 Findings, Warning Letters and Consent Decree Compliance Issues23-Feb 24-Feb Atlanta, GA, USA 12 Face to Face ComplianceOnline 
Why is FDA at my facility, and what do I do during an inspection?23-Feb 24-Feb San Diego, CA, USA 12 Face to Face ComplianceOnline 
Advertising and Promotion Regulatory Affairs Conference23-Feb 24-Feb Washington DC, USA 12 Face to Face DIA 
510(K) Submissions Workshop27-Feb 28-Feb Irvine, CA, USA 12 Face to Face Advanced Medical Technology Association (AdvaMed) 

March

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
IDE Submissions Workshop1-March 1-March Irvine, CA, USAFace to Face Advanced Medical Technology Association (AdvaMed)
PMA Submissions Workshop2-March 3-March Irvine, CA, USA 12 Face to Face Advanced Medical Technology Association (AdvaMed) 
Trade Compliance Seminar - Harmonized Tariff Schedule/Schedule B and NAFTA Rules of Origin and Documentation2-March3-March Houston, TX, USA12 Face to Face ComplianceOnline 
Understanding the FDA's Regulation of HCT/Ps and Successful Product Development Strategies2-March 3-March Boston, MA, USA 12 Face to Face ComplianceOnline 
FDA's Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies2-March3-MarchBoston, MA, USA 12 Face to Face ComplianceOnline 
The A to Z's of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals, Biologics, Medical Devices, Cosmetics, and Personal Care Products8-March 9-March San Francisco, CA, USA 12 Face to Face ComplianceOnline 
2017 FDA Forum8-March 9-March Palo Alto, CA, USA 12 Face to Face Medical Device Manufacturers Association - MDMA 
Health Policy Initiatives: Ideas Becoming Official Policy and Beyond9-March 9-March Online  Webinar Mapi Group 
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices9-March 10-March San Francisco, CA, USA 12 Face to Face ComplianceOnline 
FDA's New Import Program for 2017 - Strict Precision9-March 10-March Orlando, FL, USA 12 Face to Face ComplianceOnline 
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions13-March14-March San Francisco, CA, USA 12 Face to Face ComplianceOnline 
Medical Affairs and Scientific Communications Forum13-March 15-March Tucson, Arizona, USA 12 Face to Face DIA 
Quality and GMP Compliance for Virtual Companies (Pharmaceutical, Medical Device & Biologics Industries)16-March 17-March San Diego, CA, USA 12 Face to Face ComplianceOnline 
Data Integrity: FDA/EU Requirements and Implementation21-March 22-March Hong Kong, China 12 Face to Face ComplianceOnline 
Analytical Instrument Qualification and System Validation23-March24-March Hong Kong, China 12 Face to Face ComplianceOnline 
Managing Your FDA Inspection: Before, During and After23-March 24-March Chicago, IL, USA 12 Face to Face ComplianceOnline 
Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)30-March31-March Tampa, FL, USA 11 Face to Face ComplianceOnline 
Understanding and Implementing the New ICH/USP Elemental Impurity Guidelines30-March31-March San Francisco, CA, USA 12 Face to Face ComplianceOnline 
The New Clinical Trials Regulation and Regulatory Affairs Aspects of Medicinal Product Development in the EU30-March 31-March Zurich, Switzerland 12 Face to Face ComplianceOnline 
Understanding the Statistical Considerations for Quantitative ICH Guidelines30-March 31-March Orlando, FL, USA 12 Face to Face ComplianceOnline 

April-June

April

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
Overview of Global Regulatory Affairs - PHRMSCI_X4903-April 11-June Online 15 Online University Course University of California, Irvine Division of Continuing Education 
Training: Regulatory Affairs for Biologics5-April 6-April Washington DC, USA 12 Face to Face DIA 
Data Integrity: FDA/EU Requirements and Implementation6-April 7-April Zurich, Switzerland 12 Face to Face ComplianceOnline 
Supplier Management for Medical Device Manufacturers6-April 7-April San Francisco, CA, USA 12 Face to Face ComplianceOnline 
PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation6-April 7-April San Francisco, CA, USA 12 Face to Face ComplianceOnline 
Training: Introduction to Signal Detection and Data Mining7-April 7-April Washington DC, USA Face to Face DIA 
Health Policy Initiatives: Ideas Becoming Official Policy and Beyond9-April 9-April Online Webinar Mapi Group 
DIA Statistics Forum24-April 26-April North Bethesda, Maryland, USA 12Face to Face DIA 
CMC Workshop24-April 26-April Rockville, Maryland, USA 12Face to Face DIA

May

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
Advanced Process Validation Training - Practical Solutions and Strategies for the Medical Device Industry16-May 19-May Chicago, IL, USA 12 Face to Face Winovia LLC 

June

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
Drug Safety and Pharmacovigilance - PHRMSCI X49326-June 3-Sept Online 15 Online University Course University of California, Irvine Division of Continuing Education 

July-September

July

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
Test Method Validation Training18-July 19-July Chicago, IL, USA 12 Face to Face Winovia LLC 

May

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
         

June

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
      

October-December

October

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
       

November

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
       

December

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name