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ComplianceOnline to Host Seminar on Designing and Sustaining New and Existing Product Stability Testing Program

ComplianceOnline to Host Seminar on Designing and Sustaining New and Existing Product Stability Testing Program

ComplianceOnline Hosts Cleanroom, Microbiology & Sterility Assurance Practices Seminar for Drug & Device Manufacturers

ComplianceOnline Hosts ‘Cleanroom, Microbiology & Sterility Assurance Practices Seminar for Drug & Device Manufacturers’ News Provided By Share This Article Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers Seminar has been added to ComplianceOnline.com s offering. SAN JOSE, CA, UNITED STATES, April 15, 2021 /EINPresswire.com/ ComplianceOnline, the world’s leading provider of regulatory compliance training, is holding a 2-day virtual seminar entitled ‘Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers’ on May 10-11, 2021 (9:00 AM to 4:00 PM EDT). The seminar will be presented by Charity Ogunsanya, CEO and Founder, Pharmabiodevice Consulting LLC.

ComplianceOnline: Charity Ogunsanya Explains How to Design and Sustain New & Existing Product Stability Testing Program

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

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