09:22
Purified Water System Validation | Water System Qualification | Purified Water Generation System
03:29
Three Consecutive Batches for Validation | Why Three Batches are Considered in Validation
04:54
Hold Time Study | Hold Time Validation Study | Hold Time Validation in Pharmaceuticals
03:48
Transport Validation | Validation of Pharmaceutical Transport
03:17
How to Write a Validation Protocol | Different Parts of Validation Protocol
04:45
Validation of Cleanroom Pass Boxes | Dynamic PassBox Validation | Contamination Control by Passbox
03:58
How to Reduce Validation Costs
03:16
Revalidation of Purified Water System
03:28
Difference between Process Validation and Product Validation | Process Vs Product Validation
05:36
How to Write a Validation Master Plan
03:42
Cleaning Method Development | Development of Cleaning Procedure | Cleaning in Pharmaceuticals
06:07
Disinfectant Validation I Validation of Cleaning Agents | Disinfectant Efficacy Test
03:48
Why is Analytical Method Validation Required | Requirements of Analytical Method Validation
04:23
Basic Requirements for Process Validation
03:27
How to Effectively Execute the Validation Protocol | Execution of Validation Protocol
03:17
Importance of Validation in Pharmaceuticals
06:00
HPLC Method Validation | HPLC System Suitability | Analytical Method Validation
03:25
Procedure for Sampling in Process Validation | Sampling in Pharmaceuticals
04:34
Stratified Sampling in Process Validation | Stratified Sampling in Pharmaceuticals
03:25
Effective Swabbing Technique for Cleaning Validation | Swabbing Procedure
03:02
NOEL and MACO Calculations | Cleaning Validation Calculations
02:52
Recovery Factor of Swab
03:12
Criteria to Choose the Correct Swab
04:55
Regulatory Expectations for Cleaning Validation | FDA Requirements for Cleaning Validation
03:52
Sampling in Cleaning Validation
03:06
Worst Case Selection in Cleaning Validation | What is Worst Case in Cleaning Validation
03:36
Cleaning Validation in 10 Steps | Cleaning Validation in Pharmaceuticals | Validation of Cleaning
03:51
Difference between Generic and Branded Medicines | Types of Medicines | Generic vs Branded Medicines
08:29
Components of GMP | GMP in Pharmaceuticals | Different Parts of GMP
04:30
Fault Tree Analysis | FTA Tool for Root Cause Analysis | What is Fault Tree Analysis
05:54
Pareto Chart for Root Cause Analysis
03:59
Fishbone Diagram Tool for Root Cause Analysis | Ishikawa Diagram | Cause-and-effect Diagrams
04:13
5 Why Tool for Root Cause Analysis | 5 Why Tool with Example
03:02
5 Root Cause Analysis Tools | RCA Tools
04:30
Top 10 Indian Pharmaceutical Companies 2023 | Top 10 Pharma Companies in India
05:36
CAPA and Its Implementation | Corrective and Preventive Action in Pharmaceuticals
11:13
Investigation of Out of Specification Results | OOS Investigation
03:15
Difference between Disinfectants and Antiseptics | Disinfectants Vs Antiseptics
05:24
ALCOA and ALCOA+ in Pharmaceuticals | Principles of ALCOA | Data Integrity Principles
02:58
Aseptic Vs Sterile Conditions: What's the Difference?
04:38
10 Ways to Avoid GMP Errors | Top 10 Strategies to Prevent Manufacturing Mistakes
03:32
Difference Between Qualification and Validation | Qualification Vs Validation
08:50
Process Validation | Types of Process Validation | Process Performance Qualification
02:59
Performance Qualification (PQ) | Equipment Qualification | What is Performance Qualification
03:44
Operational Qualification (OQ) | Equipment Qualification | Qualification of Equipment
03:10
Installation Qualification (IQ) | Installation of Equipment | Qualification of Equipment
04:57
Design Qualification (DQ) | Equipment Design | Equipment Qualification
02:56
Working Principle of pH Meter | Types of pH Meter | pH Electrode Working
03:02
6 Ways to Reduce Human Errors | Human Error Prevention | Reduce GMP Errors
06:18
Tablet Manufacturing Explained : Different Stages of Tablet Manufacturing Process
04:44
Maintenance of Aseptic Conditions in Sterile Areas: Strategies for Aseptic Maintenance in Cleanrooms
08:37
Air Handling Unit and Its Working : A Step-by-Step Guide to HVAC System Functioning
08:39
GMP Violations in Indian Pharmaceutical Facilities : Causes and Consequences
06:31
GMP Requirements in Pharmaceuticals : Best Practices and Regulatory Compliance
04:44
How to write effective SOPs : Importance and Best Practices
04:39
How to Respond to FDA 483 Observations: Key Considerations and Best Practices
06:05
FDA Inspection and Compliance : Regulatory Requirements and Best Practices
03:44
Self Inspection and Quality Audits
04:49
Oral Liquid Dosage Forms
12:18
Good Laboratory Practices (GLP)
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