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A non-profit volunteer organization comprised of Regulatory Affairs professionals, OCRA has over 700 members representing more than 225 companies in Orange County and surrounding areas.

Saturday, January 21, 2017

OCRA Partnerships

If your organization would like to co-sponsor an event with OCRA or have an event promoted to OCRA Members, please review the information below.  If you believe the event meets the criteria listed below, please use the “Contact Us” feature to send your request for OCRA’s consideration.

Partnership Criteria

For the benefit of our membership, OCRA will, on occasion, partner with other nonprofit organizations to sponsor programs jointly, list other organizational events on the OCRA Website, and/or list other organizational events in the OCRA NewsBrief. In determining which activities we will co-sponsor or co-promote, the Board of Directors will consider the following:
  1. The activity should be of potential benefit or interest to OCRA members.
  2. The event should not be in direct conflict with OCRA planned programs of a similar topic.
  3. The event should not conflict with or detract from OCRA’s planned program attendance.
  4. The activity should not be a promotional or commercial event for an individual, firm, partnership, or organization.
  5. Cross-promotion is discouraged within 30 days prior to the Annual FDA-OCRA Educational Conference.
  6. Email broadcasts for events will not be sent to our members on behalf of other organizations unless OCRA is a co-sponsor of the event.
  7. Exceptions require board approval.

 Partnership Criterion for For-Profit Organizations

For-profit organizations, if offering a discount to OCRA members: Promotion requires Board approval and will be reviewed on a case-by-case basis.

TUV SUD America

Apr 21, 2016 1981
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Contact: Dr. Royth von Hahn Specialty: Devices, IVD

Kim Walker Consulting

Apr 28, 2014 1807
Contact: Kim Walker, MS, RAC (US & EU) Specialty: Devices, IVD, New Drugs/OTC,…

A Regulatory Consultants Group (RGC)

Mar 31, 2016 2853
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Contact: Trudy R. Papson Specialty: Auditing, Gap Analysis, Mock FDA Inspections for…

Consultant Directory

Jan 23, 2016 4477
This directory supplies information about consultants providing regulatory, clinical, and…

Noblitt & Rueland

May 09, 2009 4889
Contact: Brent Noblitt, Senior PartnerSpecialty: Devices, IVDs, Biologics/Biotechnology

Arivis

Jun 02, 2015 2102
arivis logo
Contact: Adair Turner, MS, RAC, Director of Regulatory and Clinical Operations…

Enterey, Inc.

Apr 21, 2016 2601
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Contact: Tita Tavares, Business Development Manager Specialty: Biologics/Biotechnology,…

Promenade Software, Inc.

Aug 26, 2016 1254
Contact: Frances Cohen, President Specialty: Devices, IVD

Strategic Regulatory Solutions, Inc.

Apr 13, 2012 16963
Contact: Gustavo Kobrin, PresidentSpecialty: Devices

Greg Godfrey & Associates

Feb 03, 2011 3091
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Contact: Greg Godfrey, RAC, CQE, CQA - Owner & Principal Consultant Specialty: Devices

Promedica International

Dec 14, 2016 360
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Contact: Terri Hopton, Manager, Business Development and Special Projects…

Quintiles Consulting

Jun 01, 2015 5601
Contact: Phil Johnson, Senior Director, Quality & Compliance Services Specialty: New and…
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