Why Should You Attend:
A successful validation program depends upon information and knowledge from product and process development. This knowledge and understanding serves as the basis for establishing an approach to the control of the manufacturing process that results in products with the desired quality attributes.
Any process design that is minimal, incomplete, lacks depth, method and/or rigor is risky business in terms of regulatory drawbacks, interrupted manufacturing operations and ultimately financial setbacks in term of company profits! Consequently, it is of utmost importance that time be put in thorough process design for product and process development (control strategy initiatives), so that the sustainable benefit of a well-designed process can be reaped for long term financial rewards and reputable status in industry based on compliance status.
The importance of establishing control strategy for processes via the understanding of the interactions between critical process parameters (CPPs) and critical quality attributes (CQAs) associated with biologics and pharmaceuticals manufacturing operations cannot be over-emphasized. The understanding of this interaction between CPPs and CQAs will subsequently facilitate the improvement of process knowledge and understanding, ultimately leading to better process control initiatives for robust manufacturing operations as well as better process validation design strategy.
Processes can be designed to easily identify any source of variation that can be promptly and efficiently corrected, subsequently minimizing waste or scraps in manufacturing processes (the FDA 2011 guideline on Process Validation). The webinar will also highlight on the 3 stages of process validation life cycle (process design, process qualification, continuous process verification) and their importance to successful and sustainable process validation program to satisfy regulatory body requirements.
Areas Covered in the Webinar:
Who Will Benefit:
From the following industries:
Victor Olatundun is a pharmaceutical professional with 25 years expertise in the field of validation, technology transfer, management consulting and quality system remediation strategy in the biologics and pharmaceutical industry. He possesses strong leadership and management skills coupled with strong technical expertise, process knowledge and understanding in the field of validation and manufacturing operations. Additionally, he possesses both hands-on expertise and a strategic view of all aspects of the validation relating to process, cleaning, shipping and commissioning & qualification projects.
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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