12:30
Zydus Vadodara Warning Letter Sep 2024 | Learning through USFDA Warning Letters
27:30
Biocon Bangalore 483's July 2024 USFDA Inspection | Learning through 483 Observations
17:32
Zydus Vadodara 483 Observation Apr 2024
11:16
Biocon Malaysia 483 Observations July 2023 | Learning from USFDA 483s
44:52
Nitrosamine Impurities-Aug 2023 NDSRIs Limit USFDA Guidance | Control of Nitrosamine Guidance Feb-21
08:09
Medgel Pharma Indore Warning Letter 20 July 2023 | Learning from USFDA Warning Letters
10:32
Baxter Pharma Warning Letter 25 July 2023 Ahmedabad | Learning from USFDA Warning Letters
19:03
Intas Pharma Warning Letter 28 July 2023 | Learning from USFDA Warning Letters | 2023 Warning Letter
05:45
QR Code for Top 300 Medicines in India | Government of India Directive to Curb counterfeit drugs
15:20
Ipca Laboratories Indore USFDA 483 June 2023 | learning from 483's
20:52
USFDA Inspections: Overview | Difference between USFDA Inspection & Other Authority Inspections
12:21
Centaur Pharma Warning Letter June 2023 USFDA | Learning from Warning Letter
01:04:14
Intas Ahmedabad 483 Observation May 2023 | Learning from 483s
35:40
IPCA Laboratories Ratlam 483 Observation June 2023 | Learning from Observations | API Facility
26:38
Revised ICH Q9 (R1) Quality Risk Management Guideline | Jan 2023
30:33
Quality Metrics Data Submission USFDA Guidance| USFDA Guidelines |
38:26
ICH Q12 Product Lifecycle Management
17:22
ICH Q3C Guidance for Residual Solvents | Class of Residual Solvents | PDE Values of Residual Solvent
25:27
21 CFR Part 11 | Electronic Records & Electronic Signatures | GxP Computer System requirements
02:19:07
Revised EU Annex 1- Manufacture of Sterile Products (25 Aug 2022) | Comprehensive Training Module
34:21
ICH Q3D Guidance for Elemental Impurities | Example for calculating | Permitted Daily Dose (PDE)
19:37
Revised Out of Specification (OOS) Guidance | USFDA Guidance | OOS Guidance May 2022
31:28
ICH Q9 Guidance for Quality Risk Management | With simplified example
19:06
USFDA Guidance for Data Integrity | USFDA Guidelines for Pharmaceutical | Easy Explanation
22:21
ICH Q10 Guidance for Pharmaceutical Quality System | Guideline for Pharmaceutical Industry
22:36
USFDA Guidance for Pharmaceutical Quality System | USFDA Guidelines for Pharmaceuticals |
04:51
How to answer the interview question on 'What are your strengths?' | Interview question
08:00
Don'ts of Interview | Things not to talk about in the interview
09:07
How to prepare for interview | Tips for Interview Preparation | 5 Steps for Interview Preparation
07:32
How to introduce youself in interview | Tell me about yourself | Describe Yourself | Interview Prep
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Presentations on Interview preparation, pharmaceutical guidelines and personal development.
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