FDA Compliance 2012 - How do I Keep FDA Happy with my Contract Manufacturer
Date2012-05-31
Deadline2012-05-31
VenuePalo Alto, USA - United States
KeywordsFDA Requirements; Contract Manufacturer; FDA Supplier Validation; Quality Program; FDA QSR; Supplier Quality; Supplier Selection
Topics/Call fo Papers
This webinar will cover techniques and process that can help you assure reliability and consistent quality from your suppliers or contract manufacturers. You will learn how to monitor your supplier and ensure they meet FDA's quality requirements.
Why Should You Attend:
No matter where a product is manufactured, quality is the responsibility of the organization whose name appears on the label. If you hire a contract manufacturer to make products that will carry your label and your name, the responsibility for the quality of that product is yours.
Areas Covered in the Seminar:
- Selection of a Contract Manufacturer.
- Auditing your Contract Manufacturer.
- Man in the Plant.
- Contractor's quality procedures.
- Contractor's analysis of raw materials, in-process, and finished products.
- Reconciliation.
- Packaging & Shipping.
- Linking responsibility to these activities.
- Batch release.
Other CFPs
- Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance
- How to Survive the FDA Design Control Inspection: Common Problems and Risk mitigation
- How to Organize and Conduct Product Complaint Investigations
- This webinar will provide you with an overview of risk factors in clinical trials and discuss possible ways to mitigate, control, assess impact, and prevent them in your trial.
- Pre-Formulation and Formulation Development of a Sound Bio Pharmaceutical Formulation that is cGMP Compliant
Last modified: 2012-04-05 20:52:51