DR. LUDWIG HUBER - Eventura

Auditing Computer Systems for FDA and International Compliance

DR. LUDWIG HUBER

Duration: 75 Minutes

Ensuring Integrity and Security of Laboratory Data for FDA / EU Compliance

DR. LUDWIG HUBER

Duration: 75 Minutes

GLP Regulations – Introduction and Strategies for Implementation

DR. LUDWIG HUBER

Duration: 75 Minutes

System Suitability Testing (SST) for USP and FDA Compliance

DR. LUDWIG HUBER

Duration: 75 Minutes

Validation and Control of Excel® Spreadsheets in Regulated Environments

DR. LUDWIG HUBER

Duration: 75 Minutes

Sampling and Sample Handling in Laboratories

DR. LUDWIG HUBER

Duration: 75 Minutes

FDA’s New Enforcement of 21 CFR Part 11

DR. LUDWIG HUBER

Duration: 75 Minutes

How to Prepare Yourself for FDA’s on-going Part 11 Inspection Program

DR. LUDWIG HUBER

Duration: 75 Minutes

Validation and Use of Excel® Spreadsheets in Regulated Environments

DR. LUDWIG HUBER

Duration: 75 Minutes

Risk Based Validation of Computer Systems and Part 11 Compliance

DR. LUDWIG HUBER

Duration: 75 Minutes

Effective Training Practices for FDA Compliance

DR. LUDWIG HUBER

Duration: 75 Minutes

Comparing GLP with GMP

DR. LUDWIG HUBER

Duration: 75 Minutes

Understanding the Final FDA Guidance for Validation of Analytical Methods

DR. LUDWIG HUBER

Duration: 75 Minutes