Any topic can be understood better with the videos, so we are working hard to create videos of important topics to help the students and professionals. Here is the list of videos created by Pharmaguideline.
We update this list regularly.
- Purified Water System Validation
- Three Consecutive Batches for Validation
- Hold Time Validation Study
- Transport Validation
- How to Write a Validation Protocol
- Validation of Cleanroom Pass Boxes
- How to Reduce Validation Costs
- Revalidation of Purified Water System
- Difference between Process Validation and Product Validation
- How to Write a Validation Master Plan
- Development of Cleaning Procedure
- Disinfectant Validation
- Why is Analytical Method Validation Required
- Basic Requirements for Process Validation
- How to Effectively Execute a Validation Protocol
- Importance of Validation in Pharmaceuticals
- HPLC Method Validation
- Procedure for Sampling in Process Validation
- Stratified Sampling in Process Validation
- Effective Swabbing Technique for Cleaning Validation
- NOEL and MACO Calculations
- Recovery Factor of Swab
- Criteria to Choose the Correct Swab
- Regulatory Expectations for Cleaning Validation
- Sampling in Cleaning Validation
- Worst Case Selection in Cleaning Validation
- Cleaning Validation in 10 Steps
- Difference between Generic and Branded Medicines
- Components of GMP
- Fault Tree Analysis
- Pareto Chart for Root Cause Analysis
- Fishbone Diagram for Root Cause Analysis
- 5 Why Tool for Root Cause Analysis
- Top 5 Root Cause Analysis Tools
- Top 10 Indian Pharmaceutical Companies
- CAPA and Its Implementation
- Investigation of OOS Results
- Disinfectants Vs Antiseptics
- ALCO & ALCOA+
- Aseptic Vs Sterile
- 10 Ways to Avoid GMP Errors
- Difference Between Qualification and Validation
- Process Validation
- Performance Qualification
- Operational Qualification
- Installation Qualification
- Design Qualification
- Working Principle of pH Meter
- 6 Ways to Reduce Human Errors
- Different Stages of Tablet Manufacturing Process
- Maintenance of Aseptic Conditions in Sterile Area
- Air Handling Unit and Its Working
- GMP Violations in Indian Pharmaceutical Facilities
- GMP Requirements in Pharmaceuticals
- How to write effective SOPs
- How to Respond to FDA 483 Observations
- FDA Inspection and Compliance
- Self Inspection and Quality Audits
- Oral Liquid Dosage Forms
- Good Laboratory Practices (GLP)
- High Performance Liquid Chromatography (HPLC)
- Prevention of Cross-contamination in Pharmaceuticals
- Top 10 Tips for Microbial Limit Test
- Basics of HVAC Systems
- Steps to Minimize the Data Integrity Risk
- Validation Master Plan (VMP)
- Purpose of Process Validation
- Analytical Method Validation
- Site Acceptance Test (SAT)
- Top 5 Tips for Interview
- Tips for Telephonic Interview
- Favorable Conditions for Microbial Growth in Cleanroom Area
- Waster Water Treatment - ETP Working
- Drug Master File - DMF in Pharmaceuticals
- Sterile Area Maintenance in Pharmaceuticals
- Difference between HPLC and GC │HPLC Vs GC
- GxP in Pharmaceuticals
- Validation Program in Pharmaceuticals
- Forced Degradation Study in Pharmaceuticals
- FDA Training Requirements
- Tips to Reduce FDA 483 Observations
- Top 6 Ways to Reduce Human Errors
- 5 Why Tool for Root Cause Investigation
- Fishbone Diagram Tool of Investigation
- Root Cause Analysis with Examples
- Basics of Cleaning Validation
- ALCOA in Pharmaceuticals
- Principle and Working of Autoclave
- Data Integrity in Pharmaceuticals
- Interview Questions and Answers for Jobs
- Good Laboratory Practices in Microbiology
- Quality Assurance vs Quality Control / QA vs QC
- Disinfectant vs Antiseptic
- Process Validation in Pharmaceutical Manufacturing
- Why do HEPA filters have 0.3 micron pore size?
- Good Manufacturing Practices - GMP in Pharmaceuticals
- Corrective and Preventive Action - CAPA
- Good Documentation Practices - GDP
- Tips to Write a Powerful CV
- Clean Room Design in Pharmaceuticals
- Air Handling Unit - AHU in Pharmaceuticals
