00:50

NDA: NEW DRUG APPLICATION

17:30

5 WHYS | WHY WHY | SIMPLIFIED!

01:11

🚀How to Up-Skill Efficiently and Achieve High Paying Positions in Pharma?

26:10

USFDA | SCORE TABLET | SPECIFICATION |

10:47

💊METHOD VALIDATION 🎯ACCURACY | TRUNESS | BIAS | RECOVERY | ...ARE THE SAME🤔❓

32:41

Q2(R2): Performance Characteristic

01:11

🚀TRANSFORM YOUR PHARMA CAREER: 2024!

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🚀TRANSFORM YOUR PHARMA CAREER: 2024!

11:17

How to prove discriminatory power of a dissolution method?

07:33

Capsule Shell: History & Size

09:05

How to Use Orthogonal Procedure to Evaluate Specificity/Selectivity?

07:13

Why Diethylene Glycol and Ethylene Glycol is Tested in Liquid Preparations?

09:05

Why High End of Reportable Range for PURITY (as % area) is just an ACCEPTANCE CRITERIA or 100%

08:40

Retention Mechanism 👉ION CHROMATOGRAPHY ✔️EXAMPLES

15:22

Retention Mechanism 👉Ion exchange chromatography ✔️EXAMPLES

11:05

Retention Mechanism 👉Ion pair chromatography✔️ EXAMPLES

18:57

Retention Mechanism ✅ RPLC ✅ NPLC✅ EXAMPLES

10:19

What questions you may ask to interviewer during a job interview?

09:46

How silica gel, a support material for HPLC column, gets produced?

22:11

How to Determine HPLC Column Volume and Porosity?

08:43

Why EPOXY is Used in PHARMA INDUSTRY?

06:00

Is adding a picture on resume a good idea?

11:56

How FBD, and Jet Milling favors NDSRI formation?

12:00

QA vs QC | PHARMA JOBS

13:17

Paper Based System vs Paperless System in the Pharma Industry

21:21

METHOD VALIDATION | REPORTABLE RANGE FOR IMPURITIES AS PER ICH Q2(R2)

21:40

METHOD VALIDATION | REPORTABLE RANGE FOR DISSOLUTION

11:36

METHOD VALIDATION | How to Define Reportable Range for Drug Product Assay and Potency?

14:31

Drug Product ASSAY vs Drug Product POTENCY

12:37

Assessing the impact of changes in test procedure on validation as per ICH Q2(R2)?

14:26

Validation During the Lifecycle of an Analytical Procedure- Q2(R2) (MFG PROCESS CHANGES- PART 2)

10:08

Validation During the Lifecycle of an Analytical Procedure As Per Q2(R2) MANUFACTURING CHANGES-1

32:41

Performance Characteristic: Validation of Analytical procedures as per ICH

15:30

General Considerations For Validation Of Analytical Procedures As Per ICH Guideline Q2(R2)

17:37

CAPA SIMPLIFIED

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VENDOR QUALIFICATION

15:25

Common Terms in GMP

15:13

OVERVIEW OF INDIAN PHARMA MARKET

12:45

What are the SKILLS required to get a job in Analytical Research and Development

13:03

What is CFR?

25:54

USFDA GMP

12:14

KEY TERMS: CLEANING VALIDATION

07:43

What is a Stability study?

08:53

Amino columns

13:05

Why Use HILIC (in Hindi)

12:01

Why use HILIC?

10:58

Why use WATER in the Normal Phase LC?

10:02

HILIC Column

08:25

Normal phase vs Reverse Phase

14:58

Why are a few “α Hydrogen Scores” not given in FDA’s & EMA’s Nitrosamine guidelines?

04:52

Tips for HPLC column cleaning

11:33

QbD vs AQbD

14:59

Common Terms Associated with QbD (QTPP, CQA, CPP, MA) with examples

10:03

HPLC Components That Affect Performance

08:45

Which Solvent is Better for Chromatography: Methanol or Acetonitrile?

10:25

Core Shell Columns

14:35

Phenyl Columns

13:26

Why acetonitrile has more elution strength than methanol in RPLC?

11:20

OOS explained in only 10 minutes!

08:56

increase in Rt for protonated base in low pH