Technical Talk_Gopal Mandloi
Welcome to Technical Talks _ Gopal Mandloi
As a part of my Personal Social Responsibility, I am on a mission to develop error-proof systems that ultimately protect patient safety.
Whatever knowledge I share on this channel is based on my experience, conceptual understanding, and logical thinking.
I do not claim this is the “only” way _ but I ensure it is the most practical, audit-ready, and industry-aligned way.
🔬 Your Trusted Source for Pharma Technical Knowledge
Here, we simplify complex pharmaceutical concepts:
GMP & Regulatory Compliance
All Validation's - PV, CV, AMV, CSV
CAPA, Deviation & Change Control
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📘 What You’ll Get
Easy-to-understand explanations
Real-world examples and case studies
Practical learning for career growth
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Interview Preparation Part 1: Must-Do Steps Before Any Job Interview
Change Control in Pharmaceuticals | Complete GMP Process, Impact Assessment & Documentation Explain
Important Announcement | Automatic Cleaning Validation Excel Sheet Freely Available | Pharma QA Tool
Automatic Cleaning Validation Excel Sheet | Calculate MACO, Swab & Rinse Limit Instant | Pharma Tool
Analytical Method Validation for Cleaning Validation Samples | Swab & Rinse Testing in Pharma QA
Campaign Length in Cleaning Validation | How to Establish Campaign Length in Pharma | QA & GMP 💯💪
Hold Time Study in Pharmaceutical Industry (GMP 2025 Guidelines | #FDA, #WHO, PIC/S Compliance)
Stratified Sampling in Process Validation | Compression Stage Explained (GMP 2025)
Episode 2: Know Your Requirement | Aapni Jarurato ko kaise samjhe |
Know Where We Are? | Financial Planning to Financial Freedom – Episode 1
URS vs FRS | What’s the Difference? | Pharma Equipment & Computer System ValidationIn
Financial Freedom upto 2028
"Process Validation in Pharmaceutical Industry (2025 GMP Guidelines) | Blend Uniformity |
Correction Factor & Purging Factor in Cleaning Validation
Cleaning Validation Automation App (Trial Version)
Process Validation | CPP | CQA | QTPP | QbD | CMA |
Process Validation in 2025 Overview for pharmaceutical
How to given weightage for worst case rating in Cleaning Validation?
How "Nitrosamine Impurities in Cleaning Validation"
Fully Automatic @Cleaning Validation
MACO Calculation for MDI & DPI Product
How to perform AMV ("Analytical Method Validation") | AMV in Hindi | Quality
Cleaning Validation Demonstration | Step-by-Step Process Explained | Cleaning Validation In Hindi
Validation, Qualification & Calibration
Validation Important Concept
APIC Guideline Cleaning validation Part -2
How to Learn Cleaning validation Easily?
Computerized System Validation- 01 of 10