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
A Day in Court: Critical Implications for Conducting Clinical Trials, presented by RAPS, with the support of AHLA 7/24/2008
       to
7/24/2008
Washington DC USA Face-to-face event

Clinical Data Acquisition Standards Harmonization (CDASH) Initiative 7/24/2008
       to
7/24/2008
Online USA Online course

PDP Testing 7/24/2008
       to
7/24/2008
Rockville MD USA Face-to-face event

The Essentials of Food and Drug Administration Medical Device Regulations: A Primer for Manufacturers and Suppliers; Part 2- Registration, Medical Device Reporting, Corrections and Removals (Recalls) 7/30/2008
       to
7/30/2008
Online USA Online course

Strategies for Postlaunch Success 7/31/2008
       to
8/1/2008
Vancouver BC CAN Face-to-face event

Resource Management at the Functional and Enterprise Levels 8/4/2008
       to
8/5/2008
Horsham PA USA Face-to-face event

Preparing Compliant eCTD Submissions 8/7/2008
       to
8/8/2008
Rockville MD USA Face-to-face event

Preparing Compliant eCTD Submissions 8/7/2008
       to
8/8/2008
Rockville MD USA Face-to-face event

Regulatory Affairs Part I and Part II -- 5 Day 8/4/2008
       to
8/8/2008
Boston MA USA Face-to-face event

Overview of Drug Development in Japan 8/11/2008
       to
8/12/2008
Bethesda MD USA Face-to-face event

Importance of Accurate Adverse Event Reporting - How to Assess the Causality Relationship 8/12/2008
       to
8/12/2008
Online USA Online course

Project Risk Management 8/11/2008
       to
8/12/2008
Horsham PA USA Face-to-face event

Overview of Drug Development 8/18/2008
       to
8/18/2008
Philadelphia PA USA Face-to-face event

Successful 510(k) Submissions 8/20/2008
       to
8/20/2008
Online USA Online course

Electronic Reporting of ICSRs & EudraVigilance 8/18/2008
       to
8/20/2008
Horsham PA USA Face-to-face event

Facilities Design and Maintenance 7/7/2008
       to
8/25/2008
Online USA Online course

European Regulatory Affairs 8/25/2008
       to
8/26/2008
Chicago IL USA Face-to-face event

DIA 6th Annual Canadian Meeting: Benefit & Risk Management: An Evolution in Progress 9/5/2008
       to
9/7/2008
Ottawa ON CAN Face-to-face event

Clinical Statistics for Nonstatisticians 9/8/2008
       to
9/9/2008
Washington DC USA Face-to-face event

Drug Safety Surveillance And Epidemiology 9/8/2008
       to
9/10/2008
Washington DC USA Face-to-face event

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

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

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

2nd DIA Conference: Oligonucleotides-based Therapeutics Conference 9/22/2008
       to
9/24/2008
Falls Church VA USA Face-to-face event

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

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

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

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