cGMP Made Easy
Pharmaceutical Due Diligence: Avoid three pharmaceutical development mistakes
13:22
cGMP Made Easy
Pharmaceutical Development: Choose the right Contract Manufacturing Organization
11:54
cGMP Made Easy
Pharmaceutical Quality by Design: When should formal documentation begin?
11:05
cGMP Made Easy
Pharmaceutical Quality by Design: Debunking three big myths (Today)
11:47
cGMP Made Easy
Corrective and Preventive Action: Three keys to inspection success
9:24
cGMP Made Easy
Quality by Design Drug Substance Correlating CQA's to Synthesis Steps made easy
14:23
cGMP Made Easy
Quality by Design Drug Substance: Critical Quality Attributes made easy
7:00
cGMP Made Easy
Pharmaceutical Quality Rsk Management: How to assess probability like a pro clone
9:01
cGMP Made Easy
Quality Risk Management: Secrets to assessing severity as easy as 1, 2, 3
9:24
cGMP Made Easy
Quality Risk Assessment: How to assess risk with limited data
9:56
cGMP Made Easy
Pharmaceutical Quality System: Does your CMO have you covered?
7:31
cGMP Made Easy
FDA Pharmaceutical Validation Guidance and ICH: What you must know
8:49
cGMP Made Easy
Pharmacetuical Quality System: Three ways to ensure effectiveness
6:48
cGMP Made Easy
Supplier Risk Management: Quality metrics that matter (4 of 8)
6:33
cGMP Made Easy
Supplier Risk Management: Are facilities maintained and orderly (5 of 8)
6:46
cGMP Made Easy
Supplier Assessment: How to know the staffing meets your needs
6:05
cGMP Made Easy
Supplier Risk Management How to assess organizational capability (3 of 8)
10:03
cGMP Made Easy
Supplier Risk Management: How to assess supply chain capability (6 of 8)
7:56
cGMP Made Easy
Supplier Risk Management: Is the quality system in control (7 of 8)
8:07
cGMP Made Easy
Supplier Risk Management: How to conduct portfolio assessments part (8 of 8)
4:43
cGMP Made Easy
Supplier Risk Management: How to define a purchasing controls system (1 of 8)
5:25
cGMP Made Easy
Supplier Risk Management: How to know the quality unit is adequate (2 of 8)
9:46
cGMP Made Easy
Why am I giving away the supplier risk management guide
1:26
cGMP Made Easy
Knowledge Assessment: What is the FDA knowledge aided assessment and structured applications (kasa}
6:16
cGMP Made Easy
Quality Culture: The CAPA System is a window into the supplier
5:24
cGMP Made Easy
CAPA Investigations: The 3 most common mistakes ( with Scope)
3:28
cGMP Made Easy
CAPA Effectiveness Checks: The 3 biggest mistakes you can avoid (Now)
3:30
cGMP Made Easy
API Process Validation: How to reduce validation costs (wow)
1:20
cGMP Made Easy
Pharmaceutical CMO Deviations: Know the sponsor responsibilities (essential)
1:19
cGMP Made Easy
Master Batch Record Requirements Drug Development (Phase 1)
2:23
cGMP Made Easy
API Expiration Date: How to extend them. (Easy Method)
2:40
cGMP Made Easy
Drug Specification Justification: Essential elements to document (Avoid Mistakes)
1:19
cGMP Made Easy
Drug Product Specifications: How to eliminate needless Out of Specification Investigations
1:28
cGMP Made Easy
Pharmaceutical equipment qualification: How QbD can reduce time and cost
1:17
cGMP Made Easy
API Manufacturing: Quality Risk Management Right-First-Time (Example)
1:27
cGMP Made Easy
Hire the right QA Pharmaceutical Consultant.
1:18
cGMP Made Easy
Risk Assessment: How to ensure valid conclusions (Today)
3:13
cGMP Made Easy
Quality Risk Management: Submission Strategy for Post-Approval Flexibility
1:28
cGMP Made Easy
Why I Don't Do Pharmaceutical Quality by Design (Not)
1:16
cGMP Made Easy
Leadership Means Being Authentic
0:28