Radiation Sterilization of Medical Products - Beyond the Basics
- Start Date:
- Thursday, 24 August, 2017
- End Date:
- Friday, 25 August, 2017 4:30pm
- Business Practice
This two day highly interactive course will cover all aspects of radiation sterilization validation, materials selection and processing implementation. This workshop has been designed to help attendees learn the ins and outs of all the radiation modalities, materials selection, and validation of the sterilization process per ISO 11137.Additionally, 483 case studies will explore how to avoid the operational and legal issues that arise from nonconformance with regulators (FDA) and auditors.
Who will Benefit:This course is designed for medical device, biologic products, and pharmaceutical professionals who desire to get a complete understanding of the validation and use of radiation sterilization for their products. Following personnel will benefit from the course:Senior quality managersSterilization managersQuality professionalsRegulatory and Compliance professionalsProduction supervisorsManufacturing engineersProduction engineersR&D engineersProcess ownersQuality engineersNote: Use coupon code REFERRAL10 and get 10% off on registration.For Registration:http://www.complianceonline.com/iso-11137-radiation-sterilization-validations-for-medical-products-seminar-training-80161SEM-prdsm?channel=meetings4docs
Conference organized by ComplianceOnline
Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality, under a code of ethics, and with process discipline to ensure greater shareholder returns.Keeping things simple and straight forward, so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.
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