Courses: Computerized Systems
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 Clinical Research |  Good ManufacturingPractices |  Quality Assurance
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On-Site Delivery
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Course Title
Available via On-Site Delivery
WEB SEMINAR: Part II - Clinical Study Reports
Available via On-Site Delivery
WEB SEMINAR: Part 1 - Non-Clinical Study Reports
Available via On-Site Delivery
WEB SEMINAR: Part III: eCTD Filing
Available via On-Site Delivery
WEB SEMINAR: Part II - Regulatory GxP Compliance Standards for SOPs
Available via On-Site Delivery
WEB SEMINAR: Part I - Generating SOPs: Perspectives and Practical Advice
Available via On-Site Delivery
WEB SEMINAR: Managing and Preparing for the New FDA Inspection
Available via On-Site Delivery
Electronic Records Compliance: A Risk-Based, Predicate Rule Approach
Available via On-Site Delivery
Validating Spreadsheets for FDA-Regulated Industry
Available via On-Site Delivery
Complying with Computer and Software Validation Requirements
Available via On-Site Delivery
Analytical Laboratory Computer Systems Validation
Available via On-Site Delivery
Complying with 21 CFR for Clinical Research
Available via On-Site Delivery
Implementing a Risk-Based Approach to Part 11 Compliance
Available via On-Site Delivery
Designing, Programming, and Assembling Process Control Instrumentation and Controllers
Available via On-Site Delivery
Available via On-Site Delivery
Available via On-Site Delivery
Validating Computerized Laboratory Instruments
Available via On-Site Delivery
Available via On-Site Delivery
Complying with FDA Requirements for Laboratory Information Management Systems (LIMS)
Available via On-Site Delivery
Auditing Computerized Laboratory and Manufacturing Operations
Available via On-Site Delivery
Implementing Good Automated Manufacturing Practices (GAMP®)
Available via On-Site Delivery