Scilife

Control Strategy Concepts - QTPP, CQA, CPP, and CMA

System validation & qualification in GMP: Key concepts explained

Good Distribution Practices (GDP) & EU Guidelines - Chapter 9 & 10

Good Distribution Practices (GDP) & EU Guidelines - Chapter 6, 7 & 8

Good Distribution Practices (GDP) & EU Guidelines - Chapter 4 & 5

Good Distribution Practices (GDP) & EU Guidelines - Part 2

Good Distribution Practices (GDP) & EU Guidelines - Part 1

Understanding EU GDP Guideline 2013/C 343/01

Key concepts of Good Distribution Practices (GDP)

Environmental monitoring and single-use technologies

How to minimize contamination in aseptic processing

Filtration and isolator technology

Round table: Best practices in Quality Management that will impact your business

Regulatory fundamentals of medical devices in the US (Part 2)

7 Principles of auditing according to ISO 19011:2018

ISO 14971:2019 The Risk Management Process for Medical Devices (Part 3)

Introduction to Corrective and Preventive Actions

System Validation and Qualification Phases

Performing Risk Management under MDR / IVDR

Document Control according to ISO 9001

How to prepare and conduct an audit

Audit program risks and opportunities according to ISO 19011:2018