Why Should You Attend:
Inefficient quality systems are costly and cumbersome to use. Your firm’s ability to be in compliance and have nimble, efficient business processes to support compliance is critical to the operational and financial success of your business. Applying the cost cutting and efficiency driving concepts of lean as it relates to quality systems will help you to make the best contribution to your firm’s long term success without sacrificing compliance and quality.
This webinar will present a practical approach to quality system continuous improvement through value stream mapping. This approach incorporates key value factors of compliance, cycle-time and user friendliness and techniques for enhancing the efficiency and usefulness of various quality systems. Value stream mapping based on the CAPA model will also be discussed during the webinar.
Areas Covered in the Webinar:
Who Will Benefit:
Philip Russ, is an experienced quality/compliance professional with 20 years’ experience in the pharmaceutical, medical device and biologics industry. He has a record of success developing and managing quality systems to support these businesses. He has a breadth of experience performing/coordinating compliance audits involving CFR210/211, CFR820, ISO13485, QSR/PAL and CMDCAS regulations.
Mr. Russ has provided expert counsel in quality systems for early development projects; pioneering drug/medical device/drug combo quality systems and compliance initiatives; designing statistical and attribute analysis programs for manufacturing processes; continuous improvement, auditing, supplier quality management, technology transfer and validation support; statistical process controls; QA expertise for development activities, design controls and GCP for both medical device and drug products.
Mr. Russ is the owner and principal consultant of ICGXP. ICGXP offers a range of regulatory compliance and quality assurance services. Inspection readiness is an expertise that Mr. Russ and his team of associates provide clients to benefit their compliance profile and foster success in the market place.
Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
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. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar 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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