Share Your Research, Maximize Your Social Impacts
Main Menu
Searching By
PARTNERS
Data Integrity 2020 - Data Integrity Practices for the Laboratory and Beyond - Webinar
Topics/Call fo Papers
Data integrity is defined as the maintenance of, and the assurance of the accuracy and consistency of, data over its entire life-cycle.
Data Integrity is a global issue with both FDA and the European Regulatory Agencies majorly focusing on the topic during compliance inspections.
Topic 1:Regulatory Guidance Review
FDA (CFR)
EU (EurdraLex)
PIC/S
Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.
Data Integrity is a global issue with both FDA and the European Regulatory Agencies majorly focusing on the topic during compliance inspections.
Topic 1:Regulatory Guidance Review
FDA (CFR)
EU (EurdraLex)
PIC/S
Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.
Other CFPs
- Risk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance Webinar
- What You Need to Know: Auditing EU-MDR and EU-IVDR Implementation
- Analytical Method Validation and Transfer According to the New FDA Guidance Training
- What You Need to Know IEC 62304 and Demystifying Software Validation using the Principles of LDLC
- Incorporating Coaching Methods Into Performance Management
Last modified: 2020-11-05 18:57:31