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Scilife @UC3eUryjS5fjxQpcaGNF-C_g@youtube.com

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04:10
Characteristics of dosage forms - Part 1
09:50
Sterility of medicinal products in manufacturing - part 2
05:13
Sterility of medicinal products in manufacturing - part 1
05:32
Supplier management according to ISO 9001:2015 (Part 2)
05:20
Supplier management according to ISO 9001:2015
06:38
How to determine auditor competence and evaluation - Clauses 7.4, 7.5 & 7.6
07:39
How to determine auditor competence and evaluation - Clauses 7.1, 7.2 & 7.3
03:34
How to conduct an audit according to ISO 19011:2018
06:58
How to conduct audit activities
04:18
How to prepare and conduct an audit
08:33
How to monitor, review and improve an audit program
04:52
How to ensure effective, efficient, and economically sound audit programs
06:24
How to assign responsibility for audits to team leaders
05:48
How to choose and determine audit methods?
03:55
How to define ISO 19011:2018 audit objectives, scope, and criteria
04:22
How to implement an audit program according to ISO 19011:2018
04:58
How to establish an audit program according to ISO 19011:2018
04:19
Roles and responsibilities in ISO 19011:2018 audit programs
04:49
Audit program risks and opportunities according to ISO 19011:2018
06:16
How to set audit program objectives according to ISO 19011:2018
07:25
How to manage an audit program according to ISO 19011:2018
08:10
What is design control?
06:03
7 Principles of auditing according to ISO 19011:2018
09:07
Key concepts of ISO 19011:2018
01:13:07
Round table: Best practices in Quality Management that will impact your business
54:09
How quality in MedTech became a driver of financial performance
01:03:58
CAPAs, events, and change control: Unlocking the potential for continuous quality improvement
52:58
Implementing Risk Based Approaches to Computerised System Validation
48:59
Managing Quality Risks in Life Sciences. Case Study: Switch from paper based to electronic QMS
01:10:32
GAMP: From theory to action in compliance management
58:32
Integrity of Quality and the Quality of Data Integrity
01:02:30
Driving Quality Culture: The Power of Your People
53:08
Practical strategies to boost your QMS document compliance
01:03:50
Leverage your audits towards digital transformation
04:36
Other physical contaminants: Intrinsic and inherent matter
04:32
Other contaminants: thermal, lightning, electromagnetic and physical
05:22
Fundamentals and types of contaminants
04:03
Contamination control
04:32
Microbial contaminants
04:20
Chemical contaminants
06:38
Clause 8: Measurement, analysis and improvement
04:16
Clause 7: Product realization (Part 1)
03:11
Clause 7: Product realization (Part 3)
04:28
Clause 7: Product realization (Part 2)
04:29
ISO 13485:2016: Key Concepts (Part 5)
04:35
ISO 13485:2016: Key Concepts (Part 4)
05:42
ISO 13485:2016: Key Concepts (Part 3)
05:25
ISO 13485:2016: Key Concepts (Part 2)
04:57
ISO 13485:2016 -Medical devices — Quality management systems. Part II (Clause 6)
03:39
ISO 13485:2016 -Medical devices — Quality management systems. Part II (Clauses 5.5 to 5.6)
04:38
ISO 13485:2016 -Medical devices — Quality management systems. Part II (Clauses 5.1 to 5.4)
05:47
ISO 13485:2016: Structure, Clauses and Key Concepts (Part 1)
05:06
Medical Device Quality Management System
04:40
ISO 13485:2016: Clauses 1 to 4
03:50
Regulatory fundamentals of medical devices in the US (Part 1)
06:29
ISO 13485:2016: Clause 0. Introduction
05:57
Regulatory fundamentals of medical devices in the US (Part 3)
03:19
Regulatory fundamentals of medical devices in the US (Part 2)
04:12
Regulatory fundamentals of medical devices in the EU (Part 1)
04:52
Regulatory fundamentals of medical devices in the US (Part 3)