Good Laboratory Practice (GLP) for Non-Clinical Laboratory Studies - Application and Compliance to Ensure Safety of Biologic Therapeutics and Medical Devices 2012

  • 19-20 Apr 2012
  • Hilton San Francisco Financial District, CA, United States

Description

Good Laboratory Practice (GLP) for Non-Clinical Laboratory Studies - Application and Compliance to Ensure Safety of Biologic Therapeutics and Medical Devices 2012 is a seminar dedicated to guidelines and strategies for conducting and managing a preclinical development program for biologic candidates (biologics, pharmaceuticals and medical devices) eventually leading to IND studies including:

  • Target areas for potential compliance infractions, resolution of audit findings, and pertinent case studies regarding the issuance of 483s and warning letters
  • Current global regulatory (FDA, ICH) directives, and the management of these mandates will ensure successful audits for compliance, and submissions

Good Laboratory Practice (GLP) for Non-Clinical Laboratory Studies - Application and Compliance to Ensure Safety of Biologic Therapeutics and Medical Devices 2012 brings together R&D investigators, Executive management, Pre-clinical and clinical, Product development, QA/ QC, Regulatory affairs, Consultants, Marketing and Training.

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Important

Please, check "Good Laboratory Practice (GLP) for Non-Clinical Laboratory Studies - Application and Compliance to Ensure Safety of Biologic Therapeutics and Medical Devices" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Medical laboratories, Pharma
Science: Life Sciences & Biology

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