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
21st Annual Workshop on Medical Communications: Defining the Future of Medical Communications 3/14/2010
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3/17/2010 		Scottsdale AZ USA Face-to-face event
Registering Drug Products in the EU: Quality (CMC) Requirements 3/16/2010
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3/18/2010 		Boston MA USA Face-to-face event
WEBINAR: FDA-CDER Discusses Activities to Reduce Preventable Medication Harm: REMS, Medication Errors, and Safe Use 3/19/2010
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3/19/2010 		USA Video/Audioconference, Webcast
Asia Medical Device Regulatory Update 3/23/2010
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3/23/2010 		Boston MA USA Face-to-face event
DIA/FDA CDER/CBER Computational Science Annual Meeting 3/22/2010
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3/23/2010 		North Bethesda MD USA Face-to-face event
Evidence-based Medicine & Health Technology Assessment: Moving From Separate Appraisals to Synergistic Communications 3/23/2010
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3/24/2010 		Washington DC USA Face-to-face event
3rd Annual Oligonucleotides-Based Therapeutic Conference 3/23/2010
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3/25/2010 		Bethesda MD USA Face-to-face event
2010 RAPS Horizons Conference & Exhibition 3/25/2010
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3/26/2010 		Baltimore MD USA Face-to-face event
FDA Guidance on Adaptive Design for Clinical Trials 3/26/2010
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3/26/2010 		Silver Spring MD USA Face-to-face event
Asia Medical Device Regulatory Update 3/29/2010
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3/29/2010 		Minneapolis MN USA Face-to-face event
WEBINAR: eCTD 101: An Overview and its Impact on the Regulatory Submissions Process 3/30/2010
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3/30/2010 		USA Video/Audioconference, Webcast
WEBINAR: Case Processing and Signal Detection: Business Process Optimization in Pharmacovigilance 3/31/2010
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3/31/2010 		USA Video/Audioconference, Webcast
Asia Medical Device Regulatory Update 3/31/2010
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3/31/2010 		San Francisco CA USA Face-to-face event
Key Issues in Enabling First in Human Studies for Stem Cell Products 4/12/2010
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4/13/2010 		North Bethesda MD USA Face-to-face event
Cardiovascular Safety in Drug Development: QT, Arrhythmias, Thrombosis, and Bleeding 4/11/2010
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4/13/2010 		Arlington VA USA Face-to-face event
4th Annual FDA/DIA Statistics Forum 4/19/2010
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4/21/2010 		North Bethesda MD USA Face-to-face event
46th DIA Annual Meeting 6/13/2010
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6/17/2010 		Washington DC USA Face-to-face event
Master of Science in Quality Assurance and Regulatory Science 7/23/2010
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7/23/2010 		Chicago IL 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
Understanding the Japanese medical device market and Pharmaceutical Affairs Law (PAL): One day course 1/8/2010
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12/4/2010 		Various USA Face-to-face event
ISO 9001:2008 Lead auditor course with emphasis on ISO 13485:2003 1/11/2010
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12/14/2010 		Various USA Face-to-face event
Implementing ISO 13485:2003: Two day course 2/1/2010
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12/15/2010 		Various USA Face-to-face event
Understanding ISO 13485:2003: One day course 1/5/2010
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12/16/2010 		Various USA Face-to-face event
Medical devices CE Marking: Three day course 1/13/2010
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12/17/2010 		Various USA Face-to-face event
ISO 13485:2003 Internal Quality Systems Auditor: Three day course 1/5/2010
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12/18/2010 		Various USA Face-to-face event
Overview of ISO 13485:2003, the CMDRs, the MDD, and JPAL: Two day course 1/11/2010
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12/22/2010 		Various USA Face-to-face event

 

Current Providers