Courses - Eventura.site

Avoid Warning Letters in View of the U.S. FDA's Stated Goal

Effective Design of Experiments (DOE) Strategies

RISK MANAGEMENT AND IMPACT ASSESSMENTS IN CHANGE CONTROL

Clinical Trial Master File (TMF) And Electronic Trial Master File (eTMF)

3-Hour Virtual Seminar on Bad Standard Operating Procedures (SOPs) – Bad Training: Garbage In, Garbage Out

ANALYTICAL METHOD VALIDATION UNDER GOOD LABORATORY PRACTICES (GLPS)

Validating and Auditing Cloud, SaaS, IaaS, PaaS Systems - Tech & Validation Trends for FDA Compliance

Developing Effective Post Market Surveillance and Complaint Handling Requirements (Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls)

Leadership in the Life Sciences - Working Effectively with Customers and Suppliers

Understanding Supply Chain Management Concepts

Understanding and Implementing a Quality by Design (QbD) Program

Regulatory Audit Preparedness

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