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Carolyn Troiano
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How to Transition from Classic Computer System Validation (CSV) to Computer Software Assurance (CSA) – Improve Both Compliance and Efficiency
watch recording
30
January
On-demand
90 Minutes
On-Demand
Pharmaceuticals
Vendor Audit Best Practices for FDA-Regulated Computer Systems in Cloud Environments and SaaS Solutions
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16
May
On-demand
90 Minutes
On-Demand
Pharmaceuticals
Business Process Mapping: Streamlining Management of Data/Records for a Clinical Trial from a Variety of Stakeholders and Systems
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1
April
On-demand
90 Minutes
On-Demand
Pharmaceuticals
Best Practices for Responding to a Form 483 Citation and/or Warning Letter Issued by FDA
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25
November
On-demand
90 Minutes
On-Demand
Pharmaceuticals
21 CFR Part 11, FDA Guidance for Electronic Records and Signatures Using a Computer System Regulated by FDA
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12
August
On-demand
90 Minutes
On-Demand
Pharmaceuticals