Why Should You Attend:
The FDA has begun to more closely scrutinize the control of outsourcing for biologicals, pharmaceuticals, and medical devices. In the Quality Systems Approach to Pharmaceutical GMP, the FDA defines outsourcing as involving hiring a second party under a contract to perform the operational processes that are part of a manufacturer’s inherent responsibilities. The International Conference on Harmonization (ICH), and the Global Harmonization Task Force (GHTF) standards also include requirements for outsourcing. The qualification of contractors for outsourcing is much more comprehensive than that required for suppliers. The same principles apply to all medical products.
Many virtual companies tend to shift responsibility from themselves to the contractor for compliance to regulatory requirements. They are often too willing to relinquish the required control over their valuable income producing assets to outsiders.
This course will help you understand your responsibilities so that you avoid regulatory problems or customer alienation that can damage your products reputation.
Areas Covered in the Webinar:
Diagrams explaining the subject matter will be provided.
Who Will Benefit:
This webinar will provide valuable assistance to all companies, especially, virtual companies who outsource the testing, manufacturing, and storage of their products / manufacturing sites.For contractors, it would help them understand their responsibilities and to gain insight into how the FDA view contractors.
Personnel in the hospital and healthcare industry would also benefit from this training.
Howard, enjoys sharing his 30 years plus experience in starting up, developing, implementing, managing, and remediating pharmaceutical and medical device quality systems. He has a BS in Biology/Chemistry and Political Science as well as work toward an MBA. His ability to quickly learn the technology is demonstrated by his success in applying quality assurance principles to a wide range of pharmaceuticals and medical devices. He is a Certified Biomedical Auditor (CBA), Certified Quality Manager (CQM), and Quality Auditor (CQA). His technical education is further complemented by his Political Science degree helping him understand the regulatory process; his work toward an MBA provides business insight. He is a member of ASQ, PDA, AAMI, RAPS, and SQA. He strongly believes that Quality is very influential in shaping successful operations. He knows how to use his leadership abilities to build organizational relationships that make systems operate effectively as well as to develop and empower people.
During experience described above, Mr. Cooper has implemented full supplier qualification systems and programs. This includes both consulting and employee roles.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).
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