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May
23

DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel

Webinar |Online Training, Wilmington, United States
May 23, 2012 | 0 people are attending

Overview: This webinar will examine the existing and proposed requirements for the FDA's DHF - including its derivative documents, the DMR and DHR. It will consider the MDD's TF/DD requirements, and evaluate the documents' differing purposes / goals. 

Organizer: 
GlobalCompliancePanel
More information about DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel »
May
24

Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanel

Webinar |Online Training, Wilmington, United States
May 24, 2012 | 0 people are attending

Overview: Analytical methods should be validated to ensure reliability, consistency and accuracy of analytical data. Method validation has been a requirement of FDA and international regulations and accreditation standards such as ISO 17025 since many years. Most often the theory is well understood but there are many questions when validation experiments are designed, conducted, and documented. 

Organizer: 
GlobalCompliancePanel
More information about Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanel »

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