ProfTalks
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11:16
Biocon Malaysia 483 Observations July 2023 | Learning from USFDA 483s
ProfTalks
887 views • 9 months ago
44:52
Nitrosamine Impurities-Aug 2023 NDSRIs Limit USFDA Guidance | Control of Nitrosamine Guidance Feb-21
ProfTalks
11K views • 9 months ago
8:09
Medgel Pharma Indore Warning Letter 20 July 2023 | Learning from USFDA Warning Letters
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727 views • 9 months ago
10:32
Baxter Pharma Warning Letter 25 July 2023 Ahmedabad | Learning from USFDA Warning Letters
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1.5K views • 9 months ago
19:03
Intas Pharma Warning Letter 28 July 2023 | Learning from USFDA Warning Letters | 2023 Warning Letter
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2.4K views • 9 months ago
5:45
QR Code for Top 300 Medicines in India | Government of India Directive to Curb counterfeit drugs
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330 views • 9 months ago
15:20
Ipca Laboratories Indore USFDA 483 June 2023 | learning from 483's
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1K views • 10 months ago
20:52
USFDA Inspections: Overview | Difference between USFDA Inspection & Other Authority Inspections
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722 views • 10 months ago
12:21
Centaur Pharma Warning Letter June 2023 USFDA | Learning from Warning Letter
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1.4K views • 10 months ago
1:04:14
Intas Ahmedabad 483 Observation May 2023 | Learning from 483s
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1K views • 10 months ago
35:40
IPCA Laboratories Ratlam 483 Observation June 2023 | Learning from Observations | API Facility
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814 views • 10 months ago
26:38
Revised ICH Q9 (R1) Quality Risk Management Guideline | Jan 2023
ProfTalks
3.2K views • 11 months ago
30:33
Quality Metrics Data Submission USFDA Guidance| USFDA Guidelines |
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976 views • 11 months ago
38:26
ICH Q12 Product Lifecycle Management
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2.1K views • 11 months ago
17:22
ICH Q3C Guidance for Residual Solvents | Class of Residual Solvents | PDE Values of Residual Solvent
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3.2K views • 1 year ago
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21 CFR Part 11 | Electronic Records & Electronic Signatures | GxP Computer System requirements
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13K views • 1 year ago
2:19:07
Revised EU Annex 1- Manufacture of Sterile Products (25 Aug 2022) | Comprehensive Training Module
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12K views • 1 year ago
34:21
ICH Q3D Guidance for Elemental Impurities | Example for calculating | Permitted Daily Dose (PDE)
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9.4K views • 1 year ago
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Revised Out of Specification (OOS) Guidance | USFDA Guidance | OOS Guidance May 2022
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9.7K views • 1 year ago
31:28
ICH Q9 Guidance for Quality Risk Management | With simplified example
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13K views • 2 years ago
19:06
USFDA Guidance for Data Integrity | USFDA Guidelines for Pharmaceutical | Easy Explanation
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4.5K views • 2 years ago
22:21
ICH Q10 Guidance for Pharmaceutical Quality System | Guideline for Pharmaceutical Industry
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10K views • 2 years ago
22:36
USFDA Guidance for Pharmaceutical Quality System | USFDA Guidelines for Pharmaceuticals |
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2.6K views • 2 years ago
4:51
How to answer the interview question on 'What are your strengths?' | Interview question
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254 views • 3 years ago
8:00
Don'ts of Interview | Things not to talk about in the interview
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How to prepare for interview | Tips for Interview Preparation | 5 Steps for Interview Preparation
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How to introduce youself in interview | Tell me about yourself | Describe Yourself | Interview Prep
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