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Pharma Quality @UC5_X6WGMCHTUg7k9zsek8uA@youtube.com

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04:08
Calibrate Your Centrifuge LIKE A PRO!
10:08
Understanding the Basics of Centrifuge in Pharma and Lab
09:00
Mastering the Calibration of Your Conductivity Meter: A Step-by-Step Guide
08:42
What is a Conductivity Meter and How Does it Work? #conductivity
06:38
Mastering Fault Tree Analysis: Step-by-Step to Effective Root Cause Discovery
09:21
Understanding Privileges in Computer Software System: Unlocking The Secrets
06:09
21 CFR Part 11 vs EU Annex 11: A Comprehensive Comparison
09:43
FMEA Explained: The Key to Proactive Risk Management
22:03
Unlocking the Secrets of Quality Risk Management for Effective Decision Making
02:24
Laboratory Practices: Avoid These 5 Common Mistakes!
24:35
Top 30 Quality Control Interview Questions Every Pharma Pro Should Know
10:34
The Ultimate Guide to pH Meter Calibration & Electrode Regeneration: Expert Tips Revealed!
07:22
pH Meters Explained: Everything You Need to Know
07:34
MASTER to remember ICH Quality Guidelines List Q1-Q14 in NO TIME!
17:28
Pharma Freshers MUST KNOW These 25 Essential Interview Questions!
11:34
CALIBRATE Your Weighing Balance LIKE A PRO in 2024? #weighingbalance
16:08
Weighing Balance Understanding: Key Role in Pharma #weighingbalance
10:32
Understanding FDA Form 483: What You Need to Know! #FDA Inspection #483 #form483 #FDA #fda483
11:50
Mastering Good Documentation Practices in Pharma: A Complete Guide
17:28
Field Alert Report (FAR) Explained: FAR Submission Process
30:34
Mastering Out of Specification (OOS) in the Pharmaceutical Industry: A Step-by-Step Guide
16:13
Ensuring Data Integrity: Alcoa++ demonstrated for Pharma Industry
11:01
Mastering Analytical Instrument Qualification USP 1058!
18:52
Cracking the Code: Simplifying EU Annex 11 Computerized System Guidelines
08:44
Fishbone Ishikawa Diagram: A Commonly Used Investigation Tool Explained
05:55
5 Why Analysis: A Commonly Used Investigation Tool Explained
18:50
Insider Insights: Best Practices for Pharma Incident Handling
16:22
A deep dive into Quality Control Laboratory in Pharmaceutical Industry
16:11
Cracking the Code: Simplifying 21 CFR Part 11 Guidelines #21cfr
06:45
Writing effective SOP: Key Elements You Need to Know I Standard Operating Procedure
18:11
HANDLING OF OUT OF CALIBRATION
04:39
Basics of Pharmacopeia: Understanding Monographs and USP-NF.
15:31
Demystifying Computerized System Validation: Top 25 Questions Answered
15:20
Mastering Deviations Handling in the Pharmaceutical Industry: A Step-by-Step Guide
18:17
Mastering Change Control Process in the Pharmaceutical Industry: A Step-by-Step Guide
16:00
Mastering Corrective and Preventive Action (CAPA) in the Pharmaceutical Industry
05:45
Maximizing Compliance: Using Traceability Matrix in Computer System Validation #16
10:26
Validation Summary Report: Your Key to Successful Computerized System Validation #15
05:32
Optimizing Performance: Qualification (PQ) in Computerized Systems #14
18:07
Mastering Operational Qualification for Computerized Systems | 21 CFR Part 11 & EU Annex 11 #13
07:40
Ensuring Compliance: Installation Qualification for Computerized Systems in Pharma #12
14:19
How to Conduct a Comprehensive Functional Risk Assessment for Computerized Systems #11
12:35
The Essential Guide to Design & Configuration Specification #10
12:44
Becoming a Validation Pro: Unlocking the Master Plan #9
02:17
VALIDATION PROJECT PLAN I CSV I COMPUTER SYSTEM VALIDATION #8
07:33
Guide to GxP Assessment for computerized system: In Pharmaceuticals #7
12:05
Supplier or Vendor Assessment: Key Steps for Computer System Validation #6
08:42
The Importance of URS in the Pharmaceutical Industry #5
13:01
The Complete Life Cycle Approach to Computerized System Validation #4
04:52
Guidance on V Model & System Life Cycle Model for Computerized System #3
05:48
Evolution of Software Categories: GAMP5 History #2
06:30
Basics of Computerized System Validation in Pharma Industry #1