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