Any topic can be understood better with the videos, so we are working to prepare videos of important topics to help the students and professionals. Here is the list of videos prepared by Pharmaguideline.
We update this list regularly.
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
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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
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
Subscribe
