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Career DevelopmentProfessional Development Portal
Professional Development Portal

Welcome to the RAPS Professional Development Portal!

This portal is designed to support your development as a regulatory professional and give you access to a full realm of educational offerings from a variety of reputable institutions and organizations. Please see the listings below for premier professional growth opportunities or search the portal using the menu on the left side of the page. You can also view a provider’s information and event listings by clicking on their logo under “Current Providers”. If you have any questions, please contact us at pdp@raps.org.

Interested in becoming a provider? You can fill out and fax the provider registration form or contact RAPS at +1 301 770 2920 x. 229 or pdp@raps.org.

To receive periodical emails informing you of new listings on the portal, please click here.

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.

Current Listings
Course Title Start & End Dates City State Country Format
Ensuring 21 CFR Part 11 compliance: Strategies for a changing environment 9/3/2008
       to
9/3/2008 		Online USA Online course
Trial Master File: Ensure Your Trial Documentation Will Pass FDA Inspection 9/3/2008
       to
9/3/2008 		Audio USA Video/Audioconference, Webcast
Structured Product Labeling Release Four: Electronic Drug Establishment Registration & Drug Listing 9/9/2008
       to
9/9/2008 		Online USA Online course
Clinical Statistics for Nonstatisticians 9/8/2008
       to
9/9/2008 		Washington DC USA Face-to-face event
Practical and Regulatory Considerations for the Implementation New Analytical Test Methods 9/9/2008
       to
9/9/2008 		Online USA Online course
Drug Safety Surveillance And Epidemiology 9/8/2008
       to
9/10/2008 		Washington DC USA Face-to-face event
Understanding and Implementing ISO 17025 - Requirements, Strategies and Tool Kits for Laboratory Accreditation 9/10/2008
       to
9/10/2008 		Online USA Online course
Internal Auditor Training for ISO 13485 Auditors 9/11/2008
       to
9/11/2008 		Online USA Online course
Immunogenicity of Therapeutic Proteins 9/10/2008
       to
9/12/2008 		Bethesda MD USA Face-to-face event
FDA Critical Path Initiative (CPI) on the Move – Complexities and Challenges 9/15/2008
       to
9/16/2008 		Bethesda MD USA Face-to-face event
2008 RAPS Annual Conference & Exhibition 9/14/2008
       to
9/17/2008 		Boston MA USA Face-to-face event
Clinical Project Management 9/15/2008
       to
9/17/2008 		Horsham PA USA Face-to-face event
Regulatory Affairs Part I: The IND Phase 9/15/2008
       to
9/17/2008 		Philadelphia PA USA Face-to-face event
Natural, Organic and Green: Ensuring FDA and USDA Compliance when "Eco-Labeling" 9/17/2008
       to
9/17/2008 		Audio Conference USA Video/Audioconference, Webcast
Fundamentals of Clinical Research Monitoring 9/15/2008
       to
9/17/2008 		Washington DC USA Face-to-face event
Leadership Experience 9/15/2008
       to
9/18/2008 		Chicago IL USA Face-to-face event
Adverse Drug Events in Premarketing Clinical Trials and Postmarketing Pharmacovigilance: The Compliance, Medical Assessment and Risk Management Continuum 9/18/2008
       to
9/19/2008 		Philadelphia PA USA Face-to-face event
90 Days Until Destruction: How to Release an FDA Import Hold 9/23/2008
       to
9/23/2008 		Audio Conference USA Video/Audioconference, Webcast
EVIDENCE-BASED MEDICINE AND HEALTH TECHNOLOGY ASSESSMENT: Can We Find Common Ground? 9/22/2008
       to
9/23/2008 		Alexandria VA USA Face-to-face event
Preparing for a U.S. FDA Audit 9/24/2008
       to
9/24/2008 		Online USA Other
Dealing with Validation Failures - Recovery Options for Failed Analytical Method and Process Validation Projects 9/24/2008
       to
9/24/2008 		Online USA Online course
Is the FDA asking too much of your 510(k)? 9/24/2008
       to
9/24/2008 		Audio Conference USA Video/Audioconference, Webcast
2nd DIA Conference: Oligonucleotides-based Therapeutics Conference 9/22/2008
       to
9/24/2008 		Falls Church VA USA Face-to-face event
Regulatory Requirements for Conducting Clinical Trials in India 9/25/2008
       to
9/25/2008 		Online USA Video/Audioconference, Webcast
What We Can Learn From Warning Letters 9/25/2008
       to
9/25/2008 		Online USA Online course
How to Establish Quality Objectives that Produce Results 9/25/2008
       to
9/25/2008 		Online USA Online course
Using Electronic Health Records and Claims Databases for Rapid-Response Pharmacovigilance Studies 9/30/2008
       to
9/30/2008 		Online USA Online course
ICSE - The Pharmaceutical Contract Services Exhibition 9/30/2008
       to
10/2/2008 		Frankfurt DEU Face-to-face event
Medical Imaging Continuum: Path Forward for Advancing the Uses of New Biopharmaceutical Products 10/2/2008
       to
10/3/2008 		Bethesda MD USA Face-to-face event
Team Building and Dynamics 10/6/2008
       to
10/7/2008 		Horsham PA USA Face-to-face event
Advanced Clinical Statistics for Nonstatisticians 10/13/2008
       to
10/14/2008 		Horsham PA USA Face-to-face event
Process Mapping - Risk-Based P&PC 10/15/2008
       to
10/15/2008 		Online USA Online course
Essentials of Project Management 10/13/2008
       to
10/15/2008 		Phoenix AZ USA Face-to-face event
DIA/PhRMA Drug Safety Conference: Planning the Lifecycle of Safety Evaluation 10/14/2008
       to
10/15/2008 		Arlington VA USA Face-to-face event
Current Advancements in Clinical Trial Disclosure: The Changing Tide 10/14/2008
       to
10/16/2008 		Chicago IL USA Face-to-face event
Portfolio, Strategy and Value Management 10/16/2008
       to
10/17/2008 		Phoenix AZ USA Face-to-face event
Regulatory Affairs Part II: The CTD/NDA Phase 10/20/2008
       to
10/22/2008 		Philadelphia PA USA Face-to-face event
Introduction to Good Clinical Practices and Auditing 10/20/2008
       to
10/22/2008 		Del Mar CA USA Face-to-face event
Project Information, Communication,and Knowledge Management 10/27/2008
       to
10/28/2008 		Horsham PA USA Face-to-face event
New Drug Prod Development & Lifecycle Management 10/29/2008
       to
10/30/2008 		Horsham PA USA Face-to-face event
DIA 6th Annual Canadian Meeting: Benefit & Risk Management: An Evolution in Progress 11/5/2008
       to
11/7/2008 		Ottawa ON CAN Face-to-face event
The 7th Annual Electronic Submissions Conference ECTD: The Adventure Continues 11/5/2008
       to
11/7/2008 		San Diego CA USA Face-to-face event
Overview of Drug Development 11/10/2008
       to
11/10/2008 		Bethesda MD USA Face-to-face event
European Regulatory Affairs 11/10/2008
       to
11/11/2008 		Washington DC USA Face-to-face event
Electronic Reporting of ICSRs & EudraVigilance 11/10/2008
       to
11/12/2008 		Horsham PA USA Face-to-face event
Leadership Experience 11/10/2008
       to
11/13/2008 		Phoenix AZ USA Face-to-face event
Executing and Controlling Projects 11/17/2008
       to
11/18/2008 		Philadelphia PA USA Face-to-face event
Fundamentals of Regulatory Affairs in Canada 11/19/2008
       to
11/20/2008 		Montreal PQ CAN Face-to-face event
Signal Detection and Data Mining: International Perspectives on Spontaneous Reports and Other Healthcare Data Sets 11/19/2008
       to
11/20/2008 		Washington DC USA Face-to-face event
Regulatory Affairs Part I: The IND Phase, Part II: The CTD/NDA Phase 11/17/2008
       to
11/20/2008 		Baltimore MD USA Face-to-face event
Graduate Certificate in Clinical Research and Regulatory Administration 7/27/2008
       to
11/30/2008 		Chicago, IL USA Face-to-face event
Introduction to the Health Product Industry 9/2/2008
       to
12/9/2008 		Weston MA USA Face-to-face event
Practical Considerations in Drug Development(formerly Advanced Topics) 12/8/2008
       to
12/10/2008 		Phoenix AZ USA Face-to-face event
RAPS Executive Development Program 6/16/2008
       to
6/19/2009 		Evanston IL USA Face-to-face event

Current Providers

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