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Other Industry Events

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 Alison Bashian at +1 440 232 0108, ext. 21.

 

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
Danube University Krems EU Regulatory Affairs Program 9/1/2011
to
12/31/2012 		Krems AUT Other
Regulatory Requirements for Medical Devices (3 units) 10/1/2011
to
10/1/2012 		USA Online course
Regulatory Requirements for Pharmaceutical Products (3 units) 10/1/2011
to
10/1/2012 		USA Online course
Regulatory Affairs Planning and Management: Concept Review and Evaluation (3 units) 10/1/2011
to
10/1/2012 		USA Online course
Regulatory Affairs for Post-Market Approval (1.5 units) 10/1/2011
to
10/1/2012 		Irvine CA USA Face-to-face event
Biomedical Business and Legal Management Essentials (3 units) 10/1/2011
to
10/1/2012 		USA Online course
Regulatory Requirements for Medical Devices ( Section 1 ) 1/9/2012
to
3/25/2012 		USA Online course
Regulatory Requirements for Pharmaceutical Products ( Section 1 ) 1/9/2012
to
3/25/2012 		USA Online course
Regulatory Affairs Planning and Management: Concept Review and Evaluation (Section 1) 1/9/2012
to
3/25/2012 		USA Online course
Biomedical Business and Legal Management Essentials ( Section 1 ) 1/9/2012
to
3/25/2012 		USA Online course
The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems 2/22/2012
to
2/23/2012 		San Francisco CA USA Face-to-face event
Global Supplier Management: Strategies for 2012 and Beyond 2/23/2012
to
2/23/2012 		USA Video/Audioconference, Webcast
Medical Communications 2012 3/5/2012
to
3/7/2012 		Champions Gate FL USA Face-to-face event
Foreign Inspections: Prepare for Increased Inspections 3/6/2012
to
3/6/2012 		USA Video/Audioconference, Webcast
7th Drug & Medical Device Litigation Forum 3/7/2012
to
3/8/2012 		Philadelphia PA USA Face-to-face event
Best Practices for Managing Export Control & Cargo Claims 3/8/2012
to
3/9/2012 		San Diego CA USA Face-to-face event
Clinical Trials Essentials: An Intensive Course 3/12/2012
to
3/16/2012 		Santa Clara CA USA Face-to-face event
Registering Drug Products in the EU: Quality (CMC) Requirements 3/13/2012
to
3/15/2012 		Cambridge MA USA Face-to-face event
Application of CAPA to the Device Sterilization Process 3/14/2012
to
3/15/2012 		Irvine CA USA Face-to-face event
PMA/510(k) Workshop & FDA Reform: 2012 and Beyond 3/21/2012
to
3/22/2012 		Cupertino CA USA Face-to-face event
Regulatory Requirements for Medical Devices 3/26/2012
to
6/10/2012 		USA Online course
Regulatory Requirements for Pharmaceutical Products 3/26/2012
to
6/10/2012 		USA Online course
Medical Device Quality Systems, CAPA and European Medical Device regulations 3/29/2012
to
3/30/2012 		Orlando FL USA Face-to-face event
Transferring a Medical OEM Molding and Assembly Operation to a Manufacturer With Validated Systems and Processes 3/29/2012
to
3/30/2012 		Chicago IL USA Face-to-face event
Regulatory Affairs for Post-Market Approval 4/9/2012
to
5/20/2012 		USA Online course
6th Annual FDA/DIA Statistics Forum 4/23/2012
to
4/25/2012 		North Bethesda MD USA Face-to-face event
Excel Spreadsheets; develop and validate for 21 CFR Part 11 compliance 4/24/2012
to
4/24/2012 		USA Video/Audioconference, Webcast
Computer System Validation - Reduce Costs and Avoid 483s 4/26/2012
to
4/27/2012 		New Orleans LA USA Face-to-face event
Biotechnology-derived “Big Molecules”: Discovery-Development-Registration 5/4/2012
to
7/15/2012 		West Lafayette IN USA Face-to-face event
Understanding and Implementing the Medical Device Directive 5/17/2012
to
5/18/2012 		Philadelphia PA USA Face-to-face event
2nd Global Pharmacovigilance & Adverse Event Reporting Conference 5/22/2012
to
5/24/2012 		Boston MA USA Face-to-face event
The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems 5/24/2012
to
5/25/2012 		NJ USA Face-to-face event
Electronic Records for Regulated Environments: Cost-Effective Approaches to Compliance 6/8/2012
to
6/9/2012 		Santa Clara CA USA Face-to-face event
Computer System Validation - Reduce Costs and Avoid 483s 6/21/2012
to
6/22/2012 		San Diego CA USA Face-to-face event
Risk Assessment-Compliance Using Easy To Fill Out Documentation 9/18/2012
to
9/18/2012 		USA Video/Audioconference, Webcast
Computer System Validation - Reduce Costs and Avoid 483s 9/20/2012
to
9/21/2012 		Philadelphia PA USA Face-to-face event

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P +1 301 770 2920     F +1 301 770 2924
Email: raps@raps.org

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