Understanding and Implementing USP <1058>: Analytical Instrument Qualification
Category: All FDA Regulated Industry , FDA Validation , Documentation and IT , Regulations & Guidances , Life Sciences , Regulatory Affairs , Common FDA Regulations

Change Control for Computer Systems - strategies and tools for FDA compliance
Category: Drugs and Chemicals (Pharma) , Medical Devices , IT control and PCI compliance , Biotechnology , All FDA Regulated Industry , Documentation and IT , Laboratory , Documentation and Policy Management , Lifescience process & Procedures , Life Sciences , Documentation and Data Management

Master Planning for Computer System Validation
Category: Medical Devices , IT control and PCI compliance , All FDA Regulated Industry , FDA Validation , Life Sciences

Managing Failure Investigations and OOS Situations - Regulatory Requirements and Strategies for Implementation
Category: Medical Devices , All FDA Regulated Industry , FDA Audit and Inspection , Life Sciences

Effective Training for FDA Compliance: What to train - How much to Train - How to Document Effectiveness
Category: Medical Devices , All FDA Regulated Industry , FDA 21 CFR Part 11 , Life Sciences

Validation of Analytical Methods and Procedures - Design, Conduct and Document for Efficiency and Compliance
Category: All FDA Regulated Industry , FDA Validation , Testing and Validation , Laboratory , Analytical Laboratory , Documentation and Policy Management , Lifescience process & Procedures , Life Sciences , Documentation and Data Management

Good Laboratory Practice Regulations
Category: Drugs and Chemicals (Pharma) , Medical Devices , Laboratory Compliance , All FDA Regulated Industry , FDA 21 CFR Part 11 , Life Sciences

Validation of Computerized Analytical Systems
Category: Drugs and Chemicals (Pharma) , Medical Devices , IT control and PCI compliance , Clinical Research , Biotechnology , All FDA Regulated Industry , Testing and Validation , Documentation and IT , Laboratory , Analytical Laboratory , Best practices , Life Sciences , Documentation and Data Management , IT

Microsoft Word and Excel in FDA Regulated Industries: Pack of Four Training Courses
Category: Drugs and Chemicals (Pharma) , Medical Devices , Documentation Manager , All FDA Regulated Industry

Risk Based Validation of Software and Computer Systems
Category: Risk Management , All FDA Regulated Industry , FDA Validation , Documentation and IT , Risk Management & Controls , All FDA Regulated Functions , Life Sciences