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Other Industry Events

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

The Professional Development Portal (PDP) 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 the related fields, to help you fulfill your professional development needs.

Many of the courses listed in the PDP have been submitted for review by RAPS and are pre-approved for RAC recertification points. For those programs that qualify, the number of RAC recertification hours available upon completion of a listing can be found under the heading, "RAC points" within the event listing page.

Interested in becoming a provider? You can fill out and fax the provider registration form or contact Alison Bashian at +1 440 232 0108, ext. 21.

 

Current Listing

Note: The number of RAC recertification hours available upon completion of a listing can be found under the heading, "RAC points" within the event listing page.

Course Title Start & End Dates City State Country Format
3rd Pharmacovigilance, Risk Management & Adverse Event Reporting 5/20/2013
to
5/22/2013 		Philadelphia PA USA Face-to-face event
Device Changes, FDA Changes, and the 510(k) 5/22/2013
to
5/22/2013 		USA Video/Audioconference, Webcast
FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials 5/23/2013
to
5/24/2013 		Tampa FL USA Face-to-face event
Key Concepts in Successful Water System Sanitization 5/23/2013
to
5/23/2013 		USA Video/Audioconference, Webcast
Device Corrections and Removals 5/28/2013
to
5/28/2013 		USA Face-to-face event
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements 5/30/2013
to
5/30/2013 		USA Video/Audioconference, Webcast
Course A: Biocompatibility of Medical Devices: Two Day Certification Course 6/3/2013
to
6/4/2013 		Brussels BEL Face-to-face event
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND 6/4/2013
to
6/4/2013 		USA Video/Audioconference, Webcast
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare 6/4/2013
to
6/4/2013 		USA Video/Audioconference, Webcast
Course B: Regulatory Toxicology of Medical Devices: An Advanced Course 6/5/2013
to
6/6/2013 		Brussels BEL Face-to-face event
Effective Training Practices for FDA Compliance 6/5/2013
to
6/5/2013 		USA Video/Audioconference, Webcast
Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations of Pharmaceutical Water Systems 6/6/2013
to
6/7/2013 		Anaheim CA USA Face-to-face event
Software Validation Planning for Executives and Managers 6/6/2013
to
6/6/2013 		USA Video/Audioconference, Webcast
Mathematics of Terminal Sterilization - Probability of Survival Approach -vs- Overkill Approach 6/11/2013
to
6/11/2013 		USA Video/Audioconference, Webcast
Auditing Analytical Laboratories for FDA Compliance 6/11/2013
to
6/11/2013 		USA Video/Audioconference, Webcast
Change Control - Key to Successful cGMP Compliance 6/12/2013
to
6/12/2013 		USA Video/Audioconference, Webcast
FDA's 21 CFR 11 Add-On Inspections - Recent Updates 6/20/2013
to
6/20/2013 		USA Video/Audioconference, Webcast
Preparing for and Surviving an FDA Inspection 6/26/2013
to
6/26/2013 		USA Video/Audioconference, Webcast
Validate your own Excel Spreadsheet Application 6/27/2013
to
6/28/2013 		Washington DC USA Face-to-face event
Complaint Handling and Management: From Receipt to Trending 6/27/2013
to
6/27/2013 		USA Video/Audioconference, Webcast
Course A: Biocompatibility of Medical Devices: Two Day Certification Course 7/8/2013
to
7/9/2013 		Philadelphia PA USA Face-to-face event
Course B: Regulatory Toxicology of Medical Devices: An Advanced Course 7/10/2013
to
7/11/2013 		Philadelphia PA USA Face-to-face event
Sustaining Effective CAPA Systems 7/10/2013
to
7/11/2013 		San Diego CA USA Face-to-face event
Statistics for the Non-Statistician 7/18/2013
to
7/19/2013 		Los Angeles CA USA Face-to-face event
6th Product and Pipeline Enhancement for Generics 7/23/2013
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7/25/2013 		Washington DC DC USA Face-to-face event
Effective Complaint Handling, Medical Device Reporting and Recalls 7/25/2013
to
7/26/2013 		Boston MA USA Face-to-face event
FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials 8/8/2013
to
8/9/2013 		Boston MA USA Face-to-face event
Statistical Considerations for ICH Guidelines 8/15/2013
to
8/16/2013 		New Orleans LA USA Face-to-face event
Clinical Trial Ethics - Right, wrong and the grey area in between 8/22/2013
to
8/23/2013 		Boston MA USA Face-to-face event
Understanding FDA and Avoiding Inspections Leading to Warning Letters, Seizures, Injunctions and Prosecutions 9/18/2013
to
9/19/2013 		Philadelphia PA USA Face-to-face event
Software Validation for the New FDA Inspections 9/19/2013
to
9/20/2013 		San Diego CA USA Face-to-face event
Molecular Basis of Manufacturing Pharmaceuticals 9/20/2013
to
12/8/2013 		West Lafayette IN USA Face-to-face event
Reduce Costs and Avoid 483s 9/26/2013
to
9/27/2013 		Philadelphia PA USA Face-to-face event
Effective Complaint Handling, Medical Device Reporting and Recalls -- Avoiding Costly Errors 9/26/2013
to
9/27/2013 		Minneapolis MN USA Face-to-face event
Statistical Analysis for Product Development 10/17/2013
to
10/18/2013 		Boston MA USA Face-to-face event

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