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cGMP Made Easy @UCCIRGoKudu3_E7rx4Krl9AA@youtube.com

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Welcome to cGMP Made Easy. If you seek answers to everyday q


13:22
Pharmaceutical Due Diligence: Avoid three pharmaceutical development mistakes
11:54
Pharmaceutical Development: Choose the right Contract Manufacturing Organization
11:05
Pharmaceutical Quality by Design: When should formal documentation begin?
11:47
Pharmaceutical Quality by Design: Debunking three big myths (Today)
09:24
Corrective and Preventive Action: Three keys to inspection success
14:23
Quality by Design Drug Substance Correlating CQA's to Synthesis Steps made easy
07:00
Quality by Design Drug Substance: Critical Quality Attributes made easy
09:01
Pharmaceutical Quality Rsk Management: How to assess probability like a pro clone
09:24
Quality Risk Management: Secrets to assessing severity as easy as 1, 2, 3
09:56
Quality Risk Assessment: How to assess risk with limited data
07:31
Pharmaceutical Quality System: Does your CMO have you covered?
08:49
FDA Pharmaceutical Validation Guidance and ICH: What you must know
06:48
Pharmacetuical Quality System: Three ways to ensure effectiveness
06:33
Supplier Risk Management: Quality metrics that matter (4 of 8)
06:46
Supplier Risk Management: Are facilities maintained and orderly (5 of 8)
06:05
Supplier Assessment: How to know the staffing meets your needs
10:03
Supplier Risk Management How to assess organizational capability (3 of 8)
07:56
Supplier Risk Management: How to assess supply chain capability (6 of 8)
08:07
Supplier Risk Management: Is the quality system in control (7 of 8)
04:43
Supplier Risk Management: How to conduct portfolio assessments part (8 of 8)
05:25
Supplier Risk Management: How to define a purchasing controls system (1 of 8)
09:46
Supplier Risk Management: How to know the quality unit is adequate (2 of 8)
01:26
Why am I giving away the supplier risk management guide
06:16
Knowledge Assessment: What is the FDA knowledge aided assessment and structured applications (kasa}
05:24
Quality Culture: The CAPA System is a window into the supplier
03:28
CAPA Investigations: The 3 most common mistakes ( with Scope)
03:30
CAPA Effectiveness Checks: The 3 biggest mistakes you can avoid (Now)
01:20
API Process Validation: How to reduce validation costs (wow)
01:19
Pharmaceutical CMO Deviations: Know the sponsor responsibilities (essential)
02:23
Master Batch Record Requirements Drug Development (Phase 1)
02:40
API Expiration Date: How to extend them. (Easy Method)
01:19
Drug Specification Justification: Essential elements to document (Avoid Mistakes)
01:28
Drug Product Specifications: How to eliminate needless Out of Specification Investigations
01:17
Pharmaceutical equipment qualification: How QbD can reduce time and cost
01:27
API Manufacturing: Quality Risk Management Right-First-Time (Example)
01:18
Hire the right QA Pharmaceutical Consultant.
03:13
Risk Assessment: How to ensure valid conclusions (Today)
01:28
Quality Risk Management: Submission Strategy for Post-Approval Flexibility
01:16
Why I Don't Do Pharmaceutical Quality by Design (Not)
00:28
Leadership Means Being Authentic