04:59

Requirement Tracebiltiy Matrix in pharmaceutical industries

15:35

Air Velocity and ACPH Calculation Test of HEPA Filters in HVAC System Qualification

12:37

Product Specific Design Approach | Basics of Steam Sterilization Cycle Development 2 of 7

09:15

Responsibilities of Quality Control Unit | in Hindi & English

02:34

How do you ensure the accuracy of fill volumes in sterile production?

03:39

Key Considerations for clean room facility design in Aseptic Area

03:38

What is the purpose of a cleanroom gowning procedure?

03:37

purpose of environmental monitoring in sterile production

02:39

Purpose of a media fill test in sterile production

07:42

Why only three batches for validation

02:25

What is the difference between aseptic and terminal sterilization techniques

02:15

How do you Prevent microbial contamination in Sterile Production

01:46

Laminar Air Flow Importance in Sterile Production

06:14

Sterilization Versus Depyrogenation in Hindi and English

05:26

Cleaning Validation | CEHT | DEHT

03:37

Sterilization Science

09:35

HVAC System Qualification Test and Rationale In Hindi and English

04:28

Dead Legs in Pharmaceutical Water System

05:39

Porous Loads and non Porous Loads in steam Sterilization

01:20

Air Over Pressure Sterilization process in Hindi and English

17:33

Overkill Design Approach in Sterilization | Basics of Steam Sterilization Cycle Development 1 of 7

03:24

Flow Chart of Moist Heat Sterilization Process Decision Tree

01:07

Guidelines for Qualification of Steam Sterilizer

11:03

Nitrogen Gas and its importance in pharmaceutical industry

09:44

Reynolds number and its importance in pharmaceutical water system

13:40

Pharmaceutical Manufacturing Terminologies

06:36

Media Fill Validation Acceptance Criteria as per EU GMP ANNEXURE 1, 2022-2023

07:09

Performance qualification of laminar air flow units

20:01

Laminar Air flow Units or LAFs and its Qualification Tests in Pharmaceutical Companies

03:56

Area classification with example of operations

18:16

Viable and non viable particle counts acceptance criteria as per EU GMP ANNEXURE 1 2022

08:44

Qualification Models V / W / X Models for Validation and Qualification

02:12

Terminal Sterilization Process or TS

05:39

Pure steam quality test

05:37

VLT or Vacuum Leak Test for Steam Sterilizer

06:31

Autoclave Performance Qualification Test Details

08:20

What is pH & its impact on parenteral preparations

15:06

EU GMP Annexure 1, Part 2 of 11, Principle of EU cGMP Annexure 1

08:00

Lyophilization Process in Pharmaceutical Companies

09:41

Pass Box in Pharmaceutical companies

13:07

Equipment Qualification Lifecycle

06:10

Why we measure only 0.5 & 5.0 micron particles in clean rooms

08:21

Viable and non viable particle counts pharmaceutical companies

12:19

Data Integrity ALCOA++ Concept

06:33

Calibration in pharmaceutical industry

03:00

Difference between validation and qualification

07:35

Media Fill Validation Process Flow Chart | MFV | APS

07:33

Installation Qualification of pharmaceutical equipment| IQ of pharmaceutical equipment

04:34

EU GMP Annexure 1, Part 1 of 11, Scope of EU GMP Annexuer 1

02:00

Terminal Sterilization of Finished Pharmaceuticals | in Hindi & English

02:38

Media Fill Validation | Aseptic Process Simulation Study

08:02

Commissioning and Qualification Approach of Validation in Hindi

06:57

Steam Sterilization basic concept Part 3 | In Hindi & English

05:49

F0 Value Calculation in steam sterilization process

11:25

Process Validation | PV and its Life cycle approach

01:48

Saturated Steam and its characteristics | in Hindi & English

07:03

Diclofenac warnings

05:29

Diclofenac side effects

05:34

Clean Rooms Classification as per regulatory guidelines

08:42

Pain Killer Diclofenac medicine and its uses