Microbiology

Microbiology

SOP for Cleaning of Oven for Depyrogenation

SOP for Oven for Depyrogenetion

SOP for Cleaning of Deep Freezer

SOP for Disposal of Empty Media Conatiner

SOP for Operating Procedure of Water Bath

SOP for Operating Procedure of Colony Counter

SOP for Microbiological Monitoring of Clean

SOP for Cleaning of DHS

SOP for Environmental Monitoring by Non Viable Air Particle Count

SOP for Environmental Monitoring of Manufacturing

Area by Settling Plate Count

SOP for Calibration of Slit – to – Agar Air Sampler

SOP for Microbiological Integrity Testing of Vials

SOP for Microscope

SOP for Cleaning of Oven for Incubator at 55°C

SOP for Heat Distribution Study in Depyrogemation Oven using Different Probes with Data Logger

SOP for Operating Procedure of Data Logger

SOP for Entering in Inoculation Room

SOP for Operating Procedure of Fogster-ULV Fogger Machine

SOP for Physical Monitoring of Microbiology Section

SOP for Cleaning of Sterile Dress Cabinet

SOP for Sterile Dress Cabinet

SOP for Operating Procedure of Culture Cabinet

SOP for Handling of Biological Indicators

SOP for METONE Laser Particle Counter

SOP for Steam Penetration Study by Bowie-Dick Test

SOP for Finger Dab

SOP for Preparation of Disinfectant Solutions

SOP for Disinfectant Efficacy Test

Maintenance of Aseptic Conditions in Pharmaceutical Sterile Areas

Difference Between Dynamic and Static Pass Box

Fungus in Pharmaceutical Cleanrooms: Types, Origins, and Decontamination

Difference Between Aseptic and Sterile Conditions

How to Eliminate Microbial Contamination from Classified Area

Risk Assessment for the Purified Water System in Pharmaceuticals

Data Integrity in Microbial Analysis

How to Remove Pathogens from Water Systems

Biocontamination Control Techniques for Purified Water System

Reynolds Number and Its Significance in Purified Water System

Biofilm Removal and Chemical Sanitization of RO Systems

Activated Carbon Filter and Increase in Efficiency for Water System

Validation of Clean Room Pass Boxes

Principle and Working of Autoclave

Media Fill Test for Sterile API Manufacturing Process

Validation of Fumigation in Cleanroom Area

Importance of Microbiological Analysis in Cleaning Method Validation

Purified Water Storage and Distribution System

Best Practices in Pharmaceutical Microbiology Laboratory.

How to Strengthen Microbiological Control of Non-Sterile Pharmaceuticals

Top 4 Problems in Sterile Pharmaceutical Manufacturing

HVAC System Validation in Pharmaceuticals | A Complete Guide to Compliance and Best Practices

Aseptic and Sterile Conditions in Pharma: Key Differences

Interview questions for freshers in the Microbiology Department:

Terminal Sterilization Methods in Pharmaceuticals

Methods of Depyrogenation in the Pharmaceutical Industry

Methods of Sterilization in the Pharmaceutical Industry

Understanding Dirty Hold Time in Pharmaceutical Equipment Cleaning

Autoclave: An Essential Sterilization Tool

“Why is Disinfectant Validation Essential in the Pharmaceutical Industry?”

“ELISA Technique: Principle, Procedure, and Applications Explained”

Understanding the Difference Between Sterile and Pyrogen-Free in Pharmaceuticals

“Why 121°C is the Ideal Temperature for Autoclave Sterilization”

what are the Instruments/Equipment’s & Accessories used in microbiology?

Role of Microbiology in Pharmaceutical industry?

Hello
Chat now via Whatsapp