FDA Compliance 2012 - How to Organize and Conduct Product Complaint Investigations
Date2012-04-26
Deadline2012-04-26
VenuePalo Alto, USA - United States
KeywordsProduct Complaint Investigations; CAPA; SOPs; root cause analysis; FDA Investigation; complaint response; social media response; crisis management; publicity
Topics/Call fo Papers
This webinar on product complaint investigations will provide the necessary information to those in food, drug, device, cosmetic and related industries that manufacture and distribute products to consumers on how to best receive, respond, investigate and correct product complaints in the best interests of the firm.
Why Should You Attend:
Every firm that manufactures FDA regulated products sold to consumers will at some time receive product complaints. What can happen when product complaints are ignored? How the firm responds to and handles the complaints is incredibly important both to the good will of the firm in the marketplace and to how FDA perceives the firm.
Who Will Benefit:
This webinar will provide valuable assistance to the following personnel:
- Quality Control/Quality Affairs
- Regulatory Affairs
- Product Development
- Engineers/chemists/biologists
- Operations/Production
Other CFPs
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- Pre-Formulation and Formulation Development of a Sound Bio Pharmaceutical Formulation that is cGMP Compliant
- Designing Effective and Efficient Extractables/Leachables Studies for Biologics
- Conducting EU Studies from a US Virtual Biotech Company
- Container Closure Systems for Liquid and Lyophilized Products
Last modified: 2012-04-05 20:42:30