2020 - Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)
Date2020-05-14 - 2020-05-15
Deadline2020-05-04
VenueBoston, MA, USA - United States
KeywordsContract Laboratories; Quality agreement; Technical agreement
Topics/Call fo Papers
In this two day workshop conference you will learn the requirements and expectations of major health care regulators that are applicable to "virtual" companies. You will learn how to diagnose your company's needs based on which GMP and GCP-governed operations you retain and which you outsource; what the current expectations and best industry practices are for selecting, qualifying and monitoring your contractors to ensure they are meeting your requirements; and how to build a quality system framework that is not excessive for your current needs, but has the structure and integration to "grow with you" as the scope your operations change in the coming months and years.
You will also learn best practices for managing a regulatory inspection, with emphasis on FDA, EMA and Health Canada, but applicable to most other major agencies as well.
You will also learn best practices for managing a regulatory inspection, with emphasis on FDA, EMA and Health Canada, but applicable to most other major agencies as well.
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Last modified: 2020-03-30 20:58:59