Designing and Sustaining New and Existing Product Stability Testing Program "Designing and Sustaining New and Existing Product Stability Testing Program" Seminar has been added to ComplianceOnline.com's offering. SAN JOSE, CA, USA, February 19, 2021 /EINPresswire.com / -- ComplianceOnline, the largest GRC advisory network, has officially launched registration for the Seminar 'Designing and Sustaining New and Existing Product Stability Testing Program'. The seminar will be held on March 3-4, 2021 (10:00 AM to 5:00 PM EST) and will be presented by Charity Ogunsanya, CEO and Founder, Pharmabiodevice Consulting. New or existing modified drug Stability Testing Program's regulations/requirements stipulated by the FDA, 21 CFR or other regulations may sometimes create an overwhelming situation based on the type of product that is being manufactured. Hence, some manufacturers of new drug products have made inadvertent mistakes in the design of their new drug stability testing program. Such mistakes may ultimately delay the new, existing, or modified product IND or NDA application process due to the data that was presented to the FDA (i.e. Relevant aspects of the stability testing program requirement may have been omitted by the drug manufacturers). It is better to understand, follow and apply the full requirements of a new product stability testing requirement from the onset or to correct an existing stability testing program to avoid future pitfalls and delayed IND or NDA submission process by the FDA.