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
  • 2016 Q4
  • 2017 Q1
  • 2017 Q2
  • 2017 Q3

Throughout the Year

TitleStart Date End DateLocationRAC CreditsTypeCompany Name
       
Regulatory Requirements for Medical Devices - EECS_X445.226 Sept 20164 Dec 2016 Online 15 Online University Course University of California, Irvine Division of Continuing Education 
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 

October-December

October

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions6-Oct 7-Oct San Francisco, CA, USA 12 Face to Face Compliance Online 
ComplianceOnline Pharma Summit 2016 – Risk Control and Compliance6-Oct 7-Oct Philadephia, PA, USA 12 Face to Face Compliance Online 
Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products6-Oct7-Oct San Francisco, CA, USA 10 Face to FaceCompliance Online 
Orphan Drugs: Oncology & Hematology11-Oct11-Oct Global Webinar Mapi Group 
Data Integrity: FDA/EU Requirements and Implementation11-Oct 12-Oct Dublin, Ireland 12 Face to Face Compliance Online 
Study Data Standards in eCTD: What You Need to Know about the New Technical Rejection Criteria12-Oct 12-Oct Online Webinar FDA CDER SBIA 
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)13-Oct 14-Oct Dublin, Ireland 12 Face to Face Compliance Online 
2nd Annual Global Regulatory Affairs CMC: Chemistry, Manufacturing and Controls Conference13-Oct 14-Oct Philadelphia, PA, USA 12 Face to Face Q1 Productions 
6th Semi-Annual European Device and Diagnostic Regulation Conference17-Oct 18-Oct Brussels, Belgium 12 Face to Face Q1 Productions 
4th Annual Promotional Review Committee Compliance & Best Practices17-Oct 18-Oct Morristown, NJ, USA 12 Face to Face ExL Events 
Analytical Methods Validation for FDA Compliance17-Oct 19-Oct Burlingame, CA, USA 12 Face to Face The Center for Professional Advancement 
Regulatory Information Management19-Oct 20-Oct Philadelphia, PA, USA Face to Face CBI, a division of UBM Americas 
FDA's Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies20-Oct 21-Oct Newark, NJ, USA 12 Face to Face Compliance Online 
Why is FDA at my facility, and what do I do during an inspection?20-Oct 21-Oct San Diego, CA, USA 12 Face to Face Compliance Online 
Design Controls for Medical Devices - Regulations, Myths, Challenges, and Best Practices20-Oct 21-Oct Chicago, IL, USA 12 Face to Face Compliance Online 
OTC Stability Program for FDA Compliance24-Oct 25-Oct Burlingame, CA, USA 12 Face to Face The Center for Professional Advancement 
Periodic Benefit Risk Evaluation Reports – Tips and Hints25-Oct 25-Oct Online Webinar Mapi Group 
Conducting Effective Quality Audits25-Oct 27-Oct New Brunswick, NJ, USA 12 Face to Face The Center for Professional Advancement 
How to Decide When a Modified Device Requires a 510(K) Clearance under New FDA Draft Guidances26-Oct 26-Oct Online Webinar Q1 Productions 
Industry at a Crossroads: Legal and Ethical Considerations of Selling Pharmaceuticals in 201627-Oct 27-Oct Online Webinar Mitchell Hamline School of Law Health Law Institute 
Statistical Analysis for Process and Product Development27-Oct 28-Oct San Francisco, CA, USA 12 Face to Face Compliance Online 
CDER Small Business and Industry Assistance (CDER SBIA) Webinar - Overview of GDUFA II and Implementation of GDUFA II User Fees28-Oct 28-Oct Online Webinar FDA | CDER | SBIA 
AdvaMed - 510(k) Submissions Workshop31-Oct 1-Nov Washington, DC, USA 12 Face to Face AdvaMed 
Product Registration and Navigating the Approval Process with Regulatory Authorities in Asia Pacific, Europe, Middle East and The Americas31-Oct 1-Nov Boston, MA, USA12 Face to Face World Compliance Seminars 

November

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
AdvaMed - IDE Submissions Workshop1-Nov 2-Nov Washington, DC, USA 12 Face to Face AdvaMed 
Computer System Validation - Reduce Costs and Avoid 483s2-Nov 3-Nov San Francisco, CA, USA 12 Face to Face Compliance Online 
21 CFR Part 11 Compliance for SaaS/Cloud Applications2-Nov 3-Nov San Francisco, CA, USA 12 Face to Face Compliance Online 
AdvaMed - PMA Submissions Workshop2-Nov 3-Nov Washington, DC, USA 12 Face to Face AdvaMed 
Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)3-Nov 4-Nov San Diego, CA, USA 12 Face to Face World Compliance Seminars 
Quality Control Laboratory Compliance - cGMPs and GLPs3-Nov 4-Nov Boston, MA, USA 11 Face to Face Compliance Online 
Change Control Best Practices - Avoiding Unintended Consequences of ChangesNov-3 Nov-4 Philadelphia, PA, USA 12 Face to Face Compliance Online 
Supplier Management for Medical Device Manufacturers10-Nov 11-Nov San Francisco, CA, USA 12 Face to Face Compliance Online 
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices10-Nov 11-Nov Boston, MA, USA 12 Face to Face Compliance Online 
FDA Recalls - Before You Start, and After You Finish10-Nov 11-Nov Tampa, FL, USA 12 Face to Face Compliance Online 
AdvaMed 7th Annual Advertising and Promotion of Medical Devices Conference 10-Nov11-NovWashington, DC, USA 12 Online Course AdvaMed 
CGMP Quality Principles for the FDA Regulated Industries10-Nov 11-Nov San Francisco, CA, USA12 Face to Face Compliance Online 
Design of Experiments for Process/Product Optimization10-Nov 11-Nov Los Angeles, CA, USA 12 Face to Face Online Compliance Panel 
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)14-Nov 15-Nov Singapore, Singapore 12 Face to Face Compliance Online 
6th Annual Medical Device Regulatory Affairs: Securing Clearance & Maintaining Compliance Conference14-Nov 15-Nov Arlington, VA, USA 12 Face to Face Q1 Productions 
Data Integrity: FDA/EU Requirements and Implementation16-Nov 17-Nov Singapore, Singapore 12 Face to Face Compliance Online 
Medical Device World 201617-Nov 18-Nov Frankfurt (Main), Germany 12 Face to Face AO Foundation 
Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs)17-Nov 18-Nov San Diego, CA, USA 11 Face to Face Compliance Online 
FDA's Import Program for 2016 - New Pathways and Pitfalls17-Nov 18-Nov Boston, MA, USA 12 Face to Face Compliance Online 
Electronic Submission Requirements for ANDAs: Are You Ready?21-Nov21-Nov Online Webinar FDA | CDER | SBIA 
How to Prepare for Pharmacovigilance (PhV) Audits & Inspections22-Nov 22-Nov Online Webinar Mapi Group 
How to Prepare for Pharmacovigilance Audits & Inspections22-Nov 22-Nov Online Webinar Mapi Group 

December

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
9th Annual Clinical Affairs and Regulatory Approvals for Diagnostics Conference5-Dec 6-Dec Alexandria, VA, USA 12Face to Face Q1 Productions 
Developing and Sustaining a Quality Culture Webinar8-Dec8-Dec Online Webinar Maetrics 
Australian Regulatory Guidelines for Medical Devices (ARGMD): Government Reimbursement, Requirements, Fees and Turnaround Time to Product Approval8-Dec 9-Dec Sydney, Australia 12 Face to Face Compliance Online 
Exploring Data Integrity To Include FDA, WHO and EMA's Latest Guidance for Industry (2015/2016)8-Dec 9-Dec Orlando, FL, USA12 Face to Face Compliance Online 
Data Integrity: FDA/EMA/TGA Requirements and Implementation8-Dec 9-Dec Sydney, Australia 12 Face to Face Compliance Onilne 
US FDA 510(k) – Latest Guidance, Due Diligence, Preparation, Submission and Clearance14-Dec 14-Dec Online Webinar Compliance Trainings 
Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency15-Dec16-Dec Salt Lake City, UT, USA 12 Face to Face Compliance Online 
The Veterinary Drug Approval Process and FDA Regulatory Oversight15-Dec 16-Dec Kansas City, MO, USA 12 Face to Face Compliance Online 

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 
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 Trials
2-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 Benefits
2-Feb 3-Feb Tampa, FL, USA Face to Face ComplianceOnline 
21 CFR Part 11 Compliance for SaaS/Cloud Applications
3-Feb 3-Feb San Diego, CA, USA 12 Face to Face ComplianceOnline 
Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products
2-Feb 3-Feb Tampa, FL, USA Face to Face ComplianceOnline 
Analytical Instrument Qualification and System Validation
7-Feb 8-Feb San Francisco, CA, USA 12 Face to Face ComplianceOnline 
SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations
9-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 Finish
9-Feb 10-Feb San Jose, CA, USA 12 Face to Face ComplianceOnline 
Understanding and Implementing a Quality by Design (QbD) Program
9-Feb10-Feb Tampa, FL, USA 12 Face to Face ComplianceOnline 
Data Integrity: FDA/EU Requirements and Implementation
13-Feb 14-Feb San Francisco, CA, USA 12 Face to Face ComplianceOnline 
FDA's Medical Device Software Regulation Strategy
16-Feb 17-Feb San Francisco, CA, USA 12 Face to Face ComplianceOnline 
Effective Design, Validation and Routine Maintenance of Pharmaceutical Water
16-Feb 17-Feb San Diego, CA, USA 12 Face to Face ComplianceOnline 
Designing and Sustaining New and Existing Product Stability Testing Program
20-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 

March

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
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 
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 
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 
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 
Health Policy Initiatives: Ideas Becoming Official Policy and Beyond9-April 9-April Online Webinar Mapi Group 

May

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
         

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
       

May

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name
         

June

TitleStart DateEnd DateLocationRAC CreditsTypeCompany Name