Conferences & TrainingOther Industry Events (PD Portal)
Other Industry Events (PD Portal)
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 RAPS at 1 301 770 2920 x. 229 or pdp@raps.org.

 

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
Clinical Trial SOPs: Ensure Your Procedures are Compliant and Followed Correctly 9/9/2010
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9/9/2010 		USA Video/Audioconference, Webcast
WEBINAR: Clinical Data Standards and Submission Compliant Deliverables: Part 1 - History, Benefits, and Implementation of Data 9/14/2010
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9/14/2010 		USA Video/Audioconference, Webcast
A Drug Recall Case Study: Lessons Learned from a Widespread Drug Recall at a Major Pharmaceutical Company 9/14/2010
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9/14/2010 		USA Video/Audioconference, Webcast
WEBINAR: Clinical Data Standards and Submission Compliant Deliverables: Part 2 - Data Standards for Regulatory Submission Deliverables 9/21/2010
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9/21/2010 		USA Video/Audioconference, Webcast
False Claims Act Liability for Pharmaceutical and Medical Device Companies: How Will Recent Changes Affect You? 9/21/2010
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9/21/2010 		USA Video/Audioconference, Webcast
How Health Care Reform and Other New Legislation Will Affect the Regulation of Advertising and Promotion 9/28/2010
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9/28/2010 		USA Video/Audioconference, Webcast
FDA's Changes to the 510(k) Process: Are You Prepared? 9/30/2010
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9/30/2010 		USA Video/Audioconference, Webcast
Global Approach to the Risk Management of Medicines 9/30/2010
       to
10/1/2010 		Washington DC USA Face-to-face event
WEBINAR: The Emergence of Digital Signatures in Clinical Operations 10/5/2010
       to
10/5/2010 		USA Video/Audioconference, Webcast
Pediatric Research in the US: Are We There Yet? 10/12/2010
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10/13/2010 		Bethesda MD USA Face-to-face event
Early Drug Development: Navigating the Treacherous Rapids 10/13/2010
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10/13/2010 		Bethesda MD USA Face-to-face event
Advancing Pediatric Research in the US 10/12/2010
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10/13/2010 		Bethesda MD USA Face-to-face event
Making the Right Investments in Biomedical Informatics for Drug Development and Healthcare 10/13/2010
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10/14/2010 		National Harbor MD USA Face-to-face event
Maternal and Pediatric Drug Safety Symposium 10/13/2010
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10/14/2010 		Bethesda MD USA Face-to-face event
Asia Medical Device Regulatory Update 10/15/2010
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10/15/2010 		Austin TX USA Face-to-face event
Partnerships to Advance Patient Recruitment and Retention in Clinical Research 10/14/2010
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10/15/2010 		Rockville MD USA Face-to-face event
Registering Drug Products in the EU: Quality (CMC) Requirements 10/13/2010
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10/15/2010 		San Mateo CA USA Face-to-face event
Asia Medical Device Regulatory Update 10/19/2010
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10/19/2010 		Princeton NJ USA Face-to-face event
Asia Medical Device Regulatory Update 10/21/2010
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10/21/2010 		Atlanta GA USA Face-to-face event
Asia Medical Device Regulatory Update 10/22/2010
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10/22/2010 		Chicago IL USA Face-to-face event
Implementing ISO 13485:2003: Two day course 8/9/2010
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10/22/2010 		Various USA Face-to-face event
2010 RAPS Annual Conference & Exhibition 10/24/2010
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10/27/2010 		San Jose CA USA Face-to-face event
DIA’s 8th Annual Canadian Meeting: “Keeping Canada on the Map: Fostering Innovation and Access to Drugs in Canada” 11/3/2010
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11/5/2010 		Ottawa ON CAN Face-to-face event
Sustaining Clinical Trial Disclosure: Going Green 11/9/2010
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11/10/2010 		Bethesda MD USA Face-to-face event
ISO 9001:2008 Lead auditor course with emphasis on ISO 13485:2003 7/19/2010
       to
12/3/2010 		Various USA Face-to-face event
US and International Prescription Drug Labeling Comparisons and Important Updates 12/8/2010
       to
12/9/2010 		Washington DC USA Face-to-face event
ISO 13485:2003 Internal Quality Systems Auditor: Three day course 8/11/2010
       to
12/15/2010 		Various USA Face-to-face event
Medical devices CE Marking: Three day course 7/19/2010
       to
12/17/2010 		Various USA Face-to-face event
Pharmacovigilance and Risk Management 2011 1/9/2011
       to
1/12/2011 		Washington DC USA Face-to-face event
CMC Workshop: Translating Science into Successful Regulatory Submissions 2/7/2011
       to
2/9/2011 		Washington DC USA Face-to-face event
Electronic Document Management 2011: The Intersection of Data, Documents and Submissions 2/15/2011
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2/17/2011 		National Harbor MD USA Face-to-face event
Marketing Pharmaceuticals 2011 2/21/2011
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2/23/2011 		Washington DC USA Face-to-face event
22nd Annual Workshop on Medical Communications 3/8/2011
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3/10/2011 		Carlsbad CA USA Face-to-face event

 

Current Providers