John Avellanet Email & Phone Number | Award winning FDA compliance expert and speaker. Co-author of the book Pharmaceutical Inspections (2014), author of Get to Market Now! Turn FDA Compliance into a Competitive Edge in the Era of Personalized Medicine (2010), co-author of the book Best Practices in Biotechnology Business Development (2008). Author of the ComplianceZen.com blog. Frequent speaker at industry events, business schools and with FDA officials. In 2006, founded the lean compliance FDA consulting firm, Cerulean Associates LLC (http://www.ceruleanllc.com). Trained as an FDA Part 11 inspector. Provides multiple, cost-effective and FDA inspection-passed quality management and data integrity consulting services to clients. See www.Ceruleanllc.com for more. Specialties: simplifying and streamlining FDA quality systems and regulatory compliance for QSR, cGMP, cGCP and cGLP, mock FDA audits and compliance gap assessments, data integrity auditing and compliance consulting (including Part 11 and Annex 11 compliance), and FDA recordkeeping and archival integrity consulting.

John Avellanet

Award winning FDA compliance expert and speaker. Co-author of the book Pharmaceutical Inspections (2...
118 Pinepoint Road, Williamsburg, United States

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John Avellanet’s Email john@ceruleanllc.com

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John Avellanet’s Location 118 Pinepoint Road, Williamsburg, United States

John Avellanet’s Current Industry Cerulean Associates

John Avellanet’s Prior Industry Philip Morris Usa | Chrysalis Technologies | Ipc Technologies

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Work Experience

Cerulean Associates

Managing Director & Principal Consultant

2006-04-01 00:00:00 - Present

Philip Morris Usa

Divisional CIO

2005-01-01 00:00:00 - 2006-04-01 00:00:00

Chrysalis Technologies

CIO

2000-11-01 00:00:00 - 2004-12-01 00:00:00

Ipc Technologies

Team Lead / Network Engineer

1997-01-01 00:00:00 - 1998-01-01 00:00:00

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FAQ About John Avellanet

John Avellanet is located at
118 Pinepoint Road, Williamsburg, United States

John Avellanet is a Award winning FDA compliance expert and speaker. Co-author of the book Pharmaceutical Inspections (2014), author of Get to Market Now! Turn FDA Compliance into a Competitive Edge in the Era of Personalized Medicine (2010), co-author of the book Best Practices in Biotechnology Business Development (2008). Author of the ComplianceZen.com blog. Frequent speaker at industry events, business schools and with FDA officials. In 2006, founded the lean compliance FDA consulting firm, Cerulean Associates LLC (http://www.ceruleanllc.com). Trained as an FDA Part 11 inspector. Provides multiple, cost-effective and FDA inspection-passed quality management and data integrity consulting services to clients. See www.Ceruleanllc.com for more. Specialties: simplifying and streamlining FDA quality systems and regulatory compliance for QSR, cGMP, cGCP and cGLP, mock FDA audits and compliance gap assessments, data integrity auditing and compliance consulting (including Part 11 and Annex 11 compliance), and FDA recordkeeping and archival integrity consulting.