Micro

Best Practices in Pharmaceutical Drainage and Drain Control
Protecting Pharmaceutical Facilities and Equipment from Foul Drain Contamination
Drainage Systems in Pharmaceutical Manufacturing: Protecting Product Integrity and Environmental Safety
Materials and Design Considerations for Pharmaceutical Drainage Systems
Microbiological and Physico-Chemical Monitoring of Pharmaceutical Drainage Systems
Qualifying Drainage Systems, Design, Installation, and Operation
Validation of Fumigation in Cleanroom Area
Biofilm Removal and Chemical Sanitization of RO Systems
Media Fill Test for Sterile API Manufacturing Process
Principle and Working of Autoclave
Validation of Clean Room Pass Boxes
Low Temperature Sterilization Process (115°C) and Its Validation
Activated Carbon Filter and Increase in Efficiency for Water System
Reynolds Number and Its Significance in Purified Water System
Sanitization of RO Membranes in Purified Water System
Importance of Microbiological Analysis in Cleaning Method Validation
What is Biofilm, Its Formation, Contamination, and Effects on Sterile Water
Biofilm Formation in Water Systems: Mechanism Overview
Procedures and Steps for Control and Removal of Biofilm in Sterile Water System
Biofilm Sensors: Types, Specifications and Uses
Standard Operating Procedure for Mechanical, Chemical, Acid Washes, and Hot Water Sanitization: Cleaning and Disinfection of Biofilm
Electrochemical Treatments for Removal of Biofilm in Pharmaceutical Sterile Water Systems
Ozonation Treatment for Biofilm Removal from Sterile Water Systems in the Pharmaceutical Industry
Ultrasound Cleaning of Biofilm for Sterile Water Systems in the Pharmaceutical Industry
Science Behind Ultrasound Cleaning & Biofilm Removal
Basics and Science Behind Ozonation for Biofilm Removal
Biocontamination Control Techniques for Purified Water System
Purified Water Storage and Distribution System
How to Remove Pathogens from Water Systems
Data Integrity in Microbial Analysis
Risk Assessment for the Purified Water System in Pharmaceuticals
How to Eliminate Microbial Contamination from Classified Area
Difference Between Aseptic and Sterile Conditions
Fungus in Pharmaceutical Cleanrooms: Types, Origins, and Decontamination
What is Disinfectant Validation?
Difference Between Dynamic and Static Pass Box
Smoke Study in Cleanroom Areas
Maintenance of Aseptic Conditions in Pharmaceutical Sterile Areas
Best Practices for Isolator Technology
The Rotation of Disinfectants Principle: True or False?
Typical Microbiology Concerns in an FDA Inspection
4 Biggest Problems in Sterile Pharmaceutical Manufacturing
How to Improve Microbiological Control of Non-Sterile Pharmaceuticals
Best Practices in Microbiology Laboratory in Pharmaceuticals
New Changes in ISO 14644-1 Classification of Air Cleanliness
Chlorination and De-chlorination of Water System
Criteria to Replace UV Lights
Biofilm and Its Formation in Water System
HVAC System Validation
Cleaning and Disinfection of a Newly Purified Water System Before Start-Up
Purified Water System
Cellulose Membrane Filters Used in Pharmaceuticals
Calibration of Heating Block
Calibration of Microscope
Calibration of Micropipettes
SOP for Operation and Calibration of Mettler Toledo Analytical Balance
SOP for Disinfectant Efficacy Test
SOP for Preparation of Disinfectant Solutions
SOP for Finger Dab
SOP for Steam Penetration Study by Bowie-Dick Test
SOP for METONE Laser Particle Counter
SOP for Handling of Biological Indicators
SOP for Operating Procedure of Culture Cabinet
SOP for Sterile Dress Cabinet
SOP for Cleaning of Sterile Dress Cabinet
SOP for Physical Monitoring of Microbiology Section
SOP for Operating Procedure of Fogster – UV Fogger Machine
SOP for Entering in Inoculation Room
SOP for Operating Procedure of Double Door Autoclave
SOP for Heat Distribution Study in Depyrogenation Oven Using Data Logger
SOP for Heat Distribution Study in Depyrogenation Oven Using Different Probes with Data Logger
SOP for Microbial Monitoring of Drainage in Solid Dosage Manufacturing Area
SOP for Cleaning of Oven for Incubator at 55°C
SOP for Oven for Incubation at 55°C
SOP for Validation of Oven for Depyrogenation
SOP for Cleaning of Oven for Depyrogenation
SOP for Oven for Depyrogenation
SOP for Cleaning of Deep Freezer
SOP for Disposal of Empty Media Container
SOP for Operating Procedure of Water Bath
SOP for Operating Procedure of Colony Counter
SOP for Microbiological Monitoring of Clean Equipment by Swab Method
SOP for Cleaning of DHS
SOP for Heat Distribution Study in Chamber of Dry Heat Sterilizer Using Different Probes with Data Logger
SOP for Validation of DHS with Biological Indicator
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 Settle Plate – Agar Air Sampler
SOP for Microbiological Integrity Testing of Vials
SOP for Cleaning of Steritest
SOP for Microscope
SOP for Identification of Contaminant in Sterile Area
SOP for Environmental Monitoring of Walk-in Incubators
SOP for Environmental Monitoring of Aseptic Area by Air Sampling for Viable Count Using Air Sampler
SOP for Sampling and Testing Schedule of Purified Water
SOP for Cleaning of Sit-to-Agar Air Sampler
SOP for Sit-to-Agar Air Sampler
SOP for Heating Block Validation
SOP for Last Test by Gel Clot Method
SOP for Investigation of Sterility Test Failure
SOP for Investigation of Out of Action Level Results of Monitoring of Microbiological Environment
SOP for Sterilization of Accessories by Dry Heat Sterilization (DHS)
SOP for Environmental Monitoring of Dispensing and Sampling Area in Raw Materials
SOP for Cleaning of Microbiological Laboratory Other Than Clean Area
SOP for Numbering System of Media
SOP for Cleaning of Microscope
SOP for Cleaning of Heating Block
SOP for Cleaning Zero Reader
SOP for Preventive Maintenance of Laminar Air Flow
SOP for Identification of Organisms
SOP for Testing of Compressed Air and Nitrogen Gas for Viable Count
SOP for Calibration of Walk-in Incubators 20-25°C and 30-35°C
SOP for Evaluation of Environmental Monitoring Results (Trend Analysis)
SOP for Testing for Bioburden of Fractional Solutions
SOP for Media Preparation
SOP for Handling of Spillage of Solid/Liquid Media Containing Growth
SOP for Disposal of Media Containing Growth
SOP for Validation of Autoclave with Biological Indicators
SOP for Maintenance and Transfer of Stock Cultures
SOP for Environmental Monitoring of Clean Area and LAF Modules
SOP for Environmental Monitoring of Aseptic Area: Finger Prints and Gown Sampling
SOP for Environmental Monitoring of Parenteral Processing Area by RODAC Plate and Swab
SOP for Entering in Sterility Testing Room
SOP for Environmental Monitoring of Aseptic Area – Non-Viable Particle Count of Air
SOP for Sampling and Testing Schedule of Water for Injection and Clean Steam
SOP for Environmental Monitoring of Parenteral Processing Area by Settling Plate Count Method
SOP for Sterility Testing
SOP for Cleaning of Vertical Autoclave
SOP for Cleaning Procedure of Balances
SOP for Validation of Microbiologist
SOP for Preparation and Bioburden Monitoring of IPA 70% v/v
SOP for Fumigation in Microbiology Lab
SOP for Disposal of Media
SOP for Micrometer
SOP for Garment Cabinet
SOP for Dynamic Pass Box
SOP for Quantification of Microbial Culture
SOP for Cleaning and Operation of Bio-safety Cabinet
SOP for Cleaning and Operation of BOD Incubator (30°C – 35°C)
SOP for Inventory and Issuance of Media
SOP for Swab Sampling for Validation of Test Surface to Evaluate Cleaning Efficacy
SOP for Cleaning of Microbiology Laboratory
SOP for Laminar Air Flow Workbench
SOP for Lyophilized Vials of Microorganisms
SOP for Preparation of Spore Coat in Biological Indicators
SOP for Identification of Culture of Microorganism
SOP for Bacteriological Incubator
SOP for Calibration BOD/Bacteriological Incubator
SOP for Calibration of Colony Counter
SOP for Validation of Autoclave with Biological Indicator for Sterilization Efficiency
SOP for Verticle Autoclave
SOP for Air Sampler
SOP for Horizontal Autoclave
SOP for Calibration of Microscope
SOP for Media Preparation and Growth Promotion Test
SOP for Identification of Micoorganisms after Subculturing
SOP for Monitoring of Raw Water and Potable Water Quality SOP for Cleaning of Refrigerator
SOP for Sterilization Reel Sealer
SOP for Post Sterility Growth Pramation Test
SOP for Inspection of Media Fill Vials and Qualification of Inspectors
SOP for Preparation of Culture Inoculum
SOP for Preparation of Dresses for Sterilization
SOP for Personnel Qualification of Aseptic Area and Sterility Testing Area
SOP for Preparation of Trends
SOP for Count Down Timer
SOP for Cleaning of Incubator
SOP for Microbial Staining Procedures
SOP for Microbial Assay
SOP for Antimicrobial Effectiveness Testing
SOP for Sterility Testing Using Manifold Filtration Method
SOP for Top Pan Balance
SOP for Disposal of Media Fill Vials after Observation
SOP for Biomerieux Kit
SOP for Cleaning of Colony Counter
SOP for Receiving the Samples in Microbiology Lab
SOP for Operation and Cleaning of Air Sampler SAS 180 L
SOP for Operation and Cleaning of Triobloc
SOP for Procedure for Bioburden, BET and LPC of Primary Packaging Materials
SOP for Operation and Cleaning of Deep Freezer
SOP for Operation and Maintenance of Fogger
SOP for Operation and Cleaning of Garment Cubicle
SOP for Operation, Cleaning and Monitoring of Laminar Air Flow
SOP for Sterility Using Streitest Equinox
SOP for Temperature, Humidity and Differential Pressure Monitoring
SOP for Collection and Testing of Samples During Process Simulation
SOP for Operation and Cleaning of Pass box
SOP for Cleaning of Glassware for Microbiology
SOP for Sampling and Testing of Pure Steam
SOP for Operation and Calibration of Micropipette
SOP for Cleaning and Operation of Anaerobic Culture Jar
SOP for Operation and Maintenance of Liquid Particle Counter
SOP for Monitoring of Microbiology Laboratory
SOP for Handling of Out of Limit Results in Environmental Monitoring and Water Analysis
SOP for Operation and Cleaning of Vertical Portable Autoclave
SOP for Handling of Out of Specification Results in Microbiological Testing
SOP for Identification of Microbial Cultures using Biomeriux Identification Systern
SOP for Testing of Biological Indicators
SOP for Bacterial Endotoxin (LAL) Test
SOP for Sterility Testing by Membrane Filtration Method
SOP for Cleaning and Sanitation of Microbiology Lab
SOP for Start up after Shut Down in Microbiology
SOP for Entry and Exit into Microbiology Testing Area and Sterility Testing Area
SOP for Monitoring of Compressed Air/ Gases
SOP for Checking Effectiveness of Disinfection/ Cleaning Procedure
SOP for Disposal of Contaminated Material
SOP for Procurement, Maintenance and Sub-culturing of Standard Microbial Cultures
SOP for Storage and Preparation of Microbiological Culture Media
SOP for Microbial Limit Test of Raw Material and Finished Product
SOP for Operation of Air Sampler
SOP for Operation, Cleaning and Monitoring of Bio-Safety Cabinet
SOP for Operation and Cleaning of Microscope
SOP for Operation and Cleaning of Steam Sterilizer
SOP for Disposal of Media Fill Vials
SOP for Proper Disposal of Contaminated Material Containing Microbial Growth
SOP for Handling of Lysate for Endotoxin Testing
SOP for Evaluation of Compressed Air in Manufacturing of Pharmaceutical Products
SOP for Personnel Monitoring for Microbial Contamination in Aseptic Area
SOP for Calibration of Micropipettes
SOP for Entry and Exit in Area for Microbiological Analysis
SOP for Cleaning of Glassware Used for Microbiological Testing
SOP for Cleaning, Maintenance and Calibration of Digital Colony Counter
SOP for Laminar Air Flow Unit
SOP for Monitoring UV Light Efficiency in LAF and Pass Box
SOP for Sterilization by Autoclave for Microbiological Analysis
SOP for Investigation of Sterility Failure to Find Out the Root Cause
SOP for Sterility Testing of Compressed Air, Nitrogen and Carbon Dioxide
SOP for Bacterial Endotoxin Test
SOP for Qualification of Biological Indicator
SOP for Maintenance and Calibration of Heating Block
SOP for Cleaning and Maintenance of Microscope
SOP for Cleaning and Maintenance of Fogger
SOP for Media Preparation for Microbial Analysis
SOP for Cleaning of Equipments in Microbiology Section
SOP for Visit the Microbiology Section
SOP for Guidelines for Working in Microbiology Laboratory
SOP for Check the Fertility Properties of the Procured Microbiological Media
SOP for Media Stock Maintenance and Suitability Testing of Media
SOP for Operation and Cleaning of Refrigerator
SOP for Entry and Exit in Microbiological Testing Room
SOP for Preparation of Culture Dilutions for Analysis
SOP for Cleaning, Operation and Calibration of Antibiotic Zone Reader
SOP for Disposal of Microbial Culture Media and Cleaning of Glassware Used for Culture Media
SOP for Microbial Analysis of Swab Samples from Equipment Surface in Production Area
SOP for Collection of Swab Sample
SOP for Palm Swabbing in Manufacturing Area
SOP for Operation and Cleaning of Autoclave
SOP for Growth Promotion Test and Calibration of Inoculum
SOP for Determination Microbial Contamination in Raw Materials and Finished Products
SOP for Sub-culturing and Maintenance of Microbial Cultures
SOP for Preparation of Microbial Culture Media
SOP for Preparation of Media Containing Sterile Petridishes, Agar Slants and Agar Butts
SOP for Cleaning and Sanitization of Microbiology Section with Disinfectants
SOP for Validation of Autoclave
SOP for Cleaning and Operation of Laminar Air Flow Workstation
SOP for Plate Exposure
SOP for Microbial Testing of Drain Water
SOP for Cleaning of Microbiological Glassware with Chromic Acid Mixture
SOP for Fumigation of Microbiology Laboratory
Isolators and Their Use in Sterile Manufacturing
GLP in Microbiology Laboratory
Environmental Isolates and Their Library in Sterile Pharmaceuticals
Difference between Sterilization and Depyrogenation
Aseptic Processing Area and Its Maintenance
Key Differences between LAF and Biological Safety Cabinet
Requirement of Active and Passive Air Sampling in Controlled Areas
Different Types of Hand Disinfectants Used in Pharmaceuticals Top 10 Tips for Microbial Limit Test
Difference between Fumigation and Fogging
Prevention of Microbial Contamination in Manufacturing
Protective Gears used in Pharmaceutical Sterile Areas
Top 10 Tips for Sterility Test
Number of Temperature Probes for Autoclave Validation
Less than 1 CFU/Plate in ISO 5 Class – How is it Possible? Favourable Conditions for Microbial Growth in
Cleanroom Area RODAC Plates and Their use in Pharmaceuticals
Why do HEPA Filters have 0.3 Micron Pore Size?
Why do We Expose Media Plates for 4 Hours in Cleanroom Areas?
Difference Between Disinfectants and Antiseptics
Different Types of Chemical Indicators for Sterilization
Difference between Incubator and BOD Incubator
Difference between Sterile and Pyrogen Free
Importance of Negative and Positive Controls in Microbial Analysis Is Fungal Count Acceptable in
Pharmaceutical Classified Area? Disinfectant Validation Protocol
Ultra Violet Light Disinfection in Pharmaceuticals
Why Petri dishes Inverted During Incubation?
Different Storage Conditions in Pharmaceuticals
Incubation Conditions for Fungus and Bacteria Using Common Media
Difference between Humidity and Relative Humidity
Microbial Resistance against Disinfectants Used for Cleaning
Handle Microbial Cultures in Separate Room
Identification of Environmental Isolates
Remove Residual Chlorine before Microbial Analysis
Microbial Analysis of Purified Water and Water of Injection
Importance and Determination of FO Value in Sterilization
Determination of Z-Value for Biological Indicators
Sterility Assurance Level (SAL) and Log Reduction (D Value) in Sterilization Why 70% Isopropyl Alcohol (IPA)
is used as Disinfectant in Pharmaceuticals?
Validation Protocol for Hold Time Study of Collected Water Samples
New VITEK MS System to Identify 193 Species of Bacteria and Yeasts Rapidly
Difference Between Purified Water and De-mineralized Water
Now Verify Sterilization Process in Two Hours with New Genetically Engineered Biological Indicators
A Different Approach to Validation and Re-validation of Washing Machine and a Depyrogenation Tunnel
Pyrogen Test and Its Determination Using Rabbits
Determination of Biological Oxygen Demand (BOD) in Waste Water
Validation Protocol for Hold Time Study of Swab Test Samples
Determination of Total Organic Carbon in Purified Water
Biological Indicator for Dry Heat Sterilization (DHS) Processes • Process Performance Qualification Protocol for Autoclave
List of Glassware Used in Pharmaceuticals
List of Chemicals and Media Required in Pharmaceuticals
Steam Sterilization (Heating in an Autoclave)
SOP for Out of Trend (OOT)
High-Efficiency Particulate Air (HEPA) and Its Significance in Sterile Pharmaceutical Preparations
lonising Radiation Sterilization
How Sterilization is done by Filtration?
What is Dry Heat sterilization (DHS)?
Validation of Shelf Life for 70% v/v Isopropyl Alcohol (IPA)
Assay of Biotin or Vitamin B7 (Biological method) in Pharmaceuticals
Microbiological Assay of Cyanocobalamin or Vitamin B12
Assay of Folic Acid or Vitamin B9 (By Microbiological Method)
Effectiveness of Antimicrobial Preservatives in Pharmaceutical Drugg
Procedure for Air Sampling (Environmental Monitoring) in Sterile Pharmaceutical Manufacturing Area
Performance Qualification of High Pressure High Vaccum (HPHV) Steam Sterilizer in Pharmaceuticals
Performance Qualification of Autoclave cum Bung Processor
Performance Qualification Protocol for Sterilization and Depyrogenating Tunnel
Purified Water Specification as per IP/BP/USP
Pyrogens Testing in Pharmaceuticals
Performance Evaluation of Biological Indicators
Biological Indicator for Moist Heat (Steam) Sterilization Processes
Types of Biological Indicators
Endotoxin Detection by End-Point Chromogenic Method
Endotoxin Detection by Kinetic Thrbidimetric and Kinetic Chromogenic Methods
Endotoxin Detection by Semi-Quantitative Gel-Clot Method
Endotoxin Detection by Gel-Clat Limit Test Method
Endotoxin Detection by Quantitative Methods
Endotoxin Detection by Gel-Clat Methods
Bacterial Endotoxin Test Methods
SOP for Octagonal Blender (1000 liter)
Sterility Validation (Membrane Filtration Method) in Pharmaceuticals
Media Fill Validation-SVP
Bacterial Endotoxin Test (BET or LAL Test) Method Validation
Clean Rooms and Controlled Areas (Sterile Area Classification)
Specification for Water for Injection (WFI) as per USP
FO Value, D Value and Z Value Calculations
SOP for Cleaning and Sterilization of Glassware Used in Microbiology Laboratory
What is HEPA filter? Its Use in Pharmaceuticals
Microbial Culture Media
HEPA Filters Used in Pharmaceuticals
UV Light Efficiency Test
Preservative Efficacy Test
Identification of Environmental Flora
Maintenance of Microbial Cultures
Investigation on Sterility Failure
Personnel Monitoring in Sterile Area
Growth Promotion Test (GPT) for Culture Media
Destruction of Microbial Waste
MLT (Microbial Limit Test) Validation
Sterility Testing by Direct Inoculation Method
Validation of Dry Heat Sterilizer (DHS)
Disinfectant Efficacy Test
MLT: Microbial Limit Test
BET: Bacterial Endotoxin (LAL) Test
Sterility Testing Procedure
Protocol for Hald Time Study of Prepared Control Standard Endotoxin (CSE)