Ethide Laboratories
Array
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[Auto Draft] => Array
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[A Comparison Of FDA And EMA Policies For EO Sterilized Devices] => Array
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[0] => EO residual testing
[1] => Medical device testing
[2] => Sterility testing
)
[Simulated Use vs. Exhaustive Extraction] => Array
(
[0] => EO residual testing
[1] => Medical device testing
)
[7 Factors That Determine Appropriate Product Sterilization] => Array
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[0] => Environmental monitoring
[1] => General
[2] => Medical device testing
[3] => Package integrity testing
[4] => Sterility testing
)
[What Products Require Ethylene Oxide Residuals Testing] => Array
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[0] => EO residual testing
[1] => Medical device testing
)
[3 Limits You Must Meet For Ethylene Oxide Residual Testing] => Array
(
[0] => EO residual testing
[1] => Medical device testing
)
[6 Components of the Chain of Infection] => Array
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[0] => Bioburden testing
[1] => General
[2] => Medical device testing
[3] => Microbiology
[4] => Sterility testing
)
[3 Key Factors That Influence EO Residual Levels] => Array
(
[0] => EO residual testing
[1] => Medical device testing
[2] => Package integrity testing
)
[Top 5 Of Things You Need To Know About Extraction Techniques For EO Residuals] => Array
(
[0] => EO residual testing
[1] => Medical device testing
)
[Overkill Method For Sterilization Validation] => Array
(
[0] => Bioburden testing
[1] => General
[2] => Medical device testing
[3] => Sterility testing
)
[5 Calculations You Need To Know To Determine EO Residuals For Your Device] => Array
(
[0] => EO residual testing
[1] => Medical device testing
)
[Medical Device Packaging Materials And Considerations For Sterilization Processes] => Array
(
[0] => Medical device testing
[1] => Package integrity testing
)
[6 Key Soil Markers For Testing Device Cleanliness] => Array
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[0] => Medical device testing
[1] => Package integrity testing
[2] => Sterility testing
)
[Bioburden and USP 62] => Array
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[0] => Bioburden testing
[1] => General
[2] => Medical device testing
[3] => Microbiology
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[Bioburden Testing For Medical Devices] => Array
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[0] => Bioburden testing
[1] => General
[2] => Medical device testing
[3] => Microbiology
[4] => Sterility testing
)
[Bioburden and USP 60] => Array
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[0] => Bioburden testing
[1] => General
[2] => Medical device testing
[3] => Microbiology
)
[Comparison Between USP 60, USP 61, And USP 62] => Array
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[0] => Bioburden testing
[1] => General
[2] => Medical device testing
[3] => Microbiology
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[Bacterial Endotoxin Testing For Medical Devices] => Array
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[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Microbiology
)
[What Are USP 61 Microbiological And Bioburden Testing Methods] => Array
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[0] => Bioburden testing
[1] => Medical device testing
[2] => Microbiology
)
[Recovery of Microorganisms For Bioburden Testing] => Array
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[0] => Bioburden testing
[1] => Medical device testing
[2] => Microbiology
)
[Neutralization of Antimicrobial Activity] => Array
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[0] => Bioburden testing
[1] => Medical device testing
[2] => Microbiology
)
[Bacterial Endotoxin vs. Bioburden Testing] => Array
(
[0] => Bacterial endotoxin testing
[1] => Bioburden testing
[2] => Medical device testing
[3] => Microbiology
)
[Special Considerations For Bacterial Endotoxin Tests For Medical Devices] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Microbiology
)
[10 Things You Need to Know About Ethylene Oxide Sterilized Medical Devices] => Array
(
[0] => EO residual testing
[1] => Medical device testing
)
[Bacterial Endotoxin Limits And Calculations For Drugs And Biologics] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
)
[Endotoxin Limits And Calculations For Medical Devices And Combination Products] => Array
(
[0] => Bacterial endotoxin testing
[1] => Cosmetic products
[2] => Medical device testing
)
[What Is Direct Contact Cytotoxicity Testing?] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
)
[What Is Agar Diffusion Test For Cytotoxicity?] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
)
[What Is An Elution Test For Cytotoxicity?] => Array
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[0] => Cytotoxicity testing
[1] => Medical device testing
)
[What Is Systemic Injection Cytotoxicity Testing For Medical Devices And Drugs?] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
)
[How Is Intracutaneous Cytotoxicity Testing Performed?] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
)
[What Is In-vivo Implantation Cytotoxicity Testing For Medical Devices And Drugs?] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
)
[Bacterial Endotoxin vs. Cytotoxicity Testing] => Array
(
[0] => Bacterial endotoxin testing
[1] => Cytotoxicity testing
[2] => Medical device testing
)
[Environmental Monitoring of Aseptic Processes] => Array
(
[0] => Aseptic processes
[1] => Environmental monitoring
[2] => Medical device testing
[3] => Microbiology
[4] => Sterility testing
)
[Bioburden vs. Cytotoxicity Testing] => Array
(
[0] => Bioburden testing
[1] => Cytotoxicity testing
[2] => Medical device testing
[3] => Microbiology
)
[Bioburden Testing vs. Microbiology Testing] => Array
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[0] => Bioburden testing
[1] => Medical device testing
[2] => Microbiology
)
[How To Control Media And Test Strains For Medical Device Testing] => Array
(
[0] => Aseptic processes
[1] => Environmental monitoring
[2] => Medical device testing
[3] => Microbiology
)
[How To Record And Evaluate Data For Regulatory Microbiology Testing] => Array
(
[0] => Aseptic processes
[1] => Environmental monitoring
[2] => Medical device testing
[3] => Microbiology
)
[How To Control Equipment And Protocols That Laboratory Technicians Use For Microbiology Testing] => Array
(
[0] => Aseptic processes
[1] => General
[2] => Medical device testing
[3] => Microbiology
)
[Bacterial Endotoxin vs. Microbiology Testing] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Microbiology
)
[How To Perform Light-obscuration Particle Matter Testing For Injectables] => Array
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[0] => Medical device testing
[1] => Microbiology
[2] => Particulate matter testing
)
[How To Perform A Microscopic Particle Count Test For Particulate Matter Within Injectables] => Array
(
[0] => Medical device testing
[1] => Microbiology
[2] => Particulate matter testing
)
[Environmental Monitoring vs. Sterilization Validation] => Array
(
[0] => Environmental monitoring
[1] => EO residual testing
[2] => Medical device testing
[3] => Sterility testing
)
[Sterility Testing Methods For Regulatory Testing] => Array
(
[0] => EO residual testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[What Types Of Pyrogens Should You Evaluate For Your Medical Device Or Medical Product?] => Array
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[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
)
[Bioburden Testing vs. Sterility Testing] => Array
(
[0] => Bioburden testing
[1] => Medical device testing
[2] => Sterility testing
)
[Bioburden Testing vs. Environmental Monitoring] => Array
(
[0] => Bioburden testing
[1] => Environmental monitoring
[2] => Medical device testing
)
[Alternatives To LAL Pyrogen Testing] => Array
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[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
)
[How To Measure Endotoxins In Medical Products] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Microbiology
[3] => Parenteral products
[4] => Pyrogenicity testing
)
[Pyrogens vs. Bacterial Endotoxins For Regulatory Testing] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Microbiology
[3] => Pyrogenicity testing
)
[Cytotoxicity Testing Vs. EO Residual Testing] => Array
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[0] => Cytotoxicity testing
[1] => EO residual testing
[2] => Medical device testing
)
[How To Perform Microbiology Testing For Nutritional & Dietary Supplements] => Array
(
[0] => General
[1] => Medical device testing
[2] => Microbiology
)
[EO Residual Testing Vs. Sterilization Validations Vs. Sterility Testing] => Array
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[0] => EO residual testing
[1] => Medical device testing
[2] => Sterility testing
)
[What Are The Current Issues With Electronic Particle Counters?] => Array
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[0] => Medical device testing
[1] => Microbiology
[2] => Parenteral products
[3] => Particulate matter testing
)
[How Are Microbial Characterizations For Microbiology Testing] => Array
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[0] => Medical device testing
[1] => Microbiology
)
[How To Perform Particulate Matter Testing For Ophthalmic Solutions] => Array
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[0] => Medical device testing
[1] => Microbiology
[2] => Parenteral products
[3] => Particulate matter testing
)
[USP 788 Particulate Matter Testing Methods] => Array
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[0] => Medical device testing
[1] => Microbiology
[2] => Parenteral products
[3] => Particulate matter testing
)
[How To Control Endotoxins In Medical Products] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Microbiology
)
[Sampling For Sterility Testing] => Array
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[0] => Medical device testing
[1] => Sterility testing
)
[Sterilization Validations vs. EO Residual Testing] => Array
(
[0] => EO residual testing
[1] => Medical device testing
[2] => Sterility testing
)
[How To Perform Environmental Monitoring For Sterility Assurance] => Array
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[0] => Environmental monitoring
[1] => Medical device testing
[2] => Sterility testing
)
[Environmental Monitoring Of Non-Sterile Processes] => Array
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[0] => Environmental monitoring
[1] => Medical device testing
[2] => Sterility testing
)
[Subvisible Particle Detection Within Traditional Parenteral Products Vs. Therapeutic Protein Biologics] => Array
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[0] => Medical device testing
[1] => Microbiology
[2] => Parenteral products
[3] => Particulate matter testing
)
[How To Test For Subvisible Particles In Therapeutic Protein Injections] => Array
(
[0] => Medical device testing
[1] => Microbiology
[2] => Parenteral products
[3] => Particulate matter testing
)
[Sterilization Validations vs. Sterility Testing] => Array
(
[0] => Medical device testing
[1] => Sterility testing
)
[Sterilization Vs. Pasteurization For Parenteral Products] => Array
(
[0] => Medical device testing
[1] => Parenteral products
[2] => Sterility testing
)
[Bioburden Vs. Biofilms For Medical Device Testing] => Array
(
[0] => Bioburden testing
[1] => Medical device testing
)
[USP 1111 Guidelines & Limits For Bioburden] => Array
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[0] => Bioburden testing
[1] => Good manufacturing practices
[2] => Medical device testing
)
[D Value Vs. Z Value Calculations For Medical Devices & Product Sterilization] => Array
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[0] => Bioburden testing
[1] => Medical device testing
[2] => Sterility testing
)
[F Value Calculations For Medical Device And Product Sterilization] => Array
(
[0] => Medical device testing
[1] => Sterility testing
)
[Sterilization By Dry Heat For Medical Devices & Products] => Array
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[0] => Medical device testing
[1] => Pyrogenicity testing
[2] => Sterility testing
)
[Sterilization By Filtration For Parenteral & Biologic Products] => Array
(
[0] => Medical device testing
[1] => Parenteral products
[2] => Sterility testing
)
[Microbiology Testing Vs. Environmental Monitoring] => Array
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[0] => Environmental monitoring
[1] => Medical device testing
[2] => Microbiology
)
[Sterilization Of Bacteria, Fungi And Virus For Medical Devices] => Array
(
[0] => Bioburden testing
[1] => Medical device testing
[2] => Sterility testing
)
[Sterilization By Radiation] => Array
(
[0] => Medical device testing
[1] => Parenteral products
[2] => Sterility testing
)
[Sterilization By Moist Heat] => Array
(
[0] => Medical device testing
[1] => Parenteral products
[2] => Sterility testing
)
[Sterilization By Ethylene Oxide (EO) For Medical Devices] => Array
(
[0] => EO residual testing
[1] => Medical device testing
[2] => Sterility testing
)
[Why Are Bacterial Spores Hard To Sterilize?] => Array
(
[0] => Aseptic processes
[1] => Bioburden testing
[2] => Medical device testing
[3] => Sterility testing
)
[Steam Sterilization Vs. Dry Heat Sterilization For Medical Devices & Products] => Array
(
[0] => Aseptic processes
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
[4] => Sterility testing
)
[Bacterial Endotoxin Testing Vs. Environmental Monitoring] => Array
(
[0] => Aseptic processes
[1] => Bacterial endotoxin testing
[2] => Environmental monitoring
[3] => Medical device testing
)
[Environmental Monitoring Vs. Ethylene Oxide (EO) Residual Testing] => Array
(
[0] => Aseptic processes
[1] => Environmental monitoring
[2] => EO residual testing
[3] => Medical device testing
[4] => Sterility testing
)
[Cytotoxicity Testing Vs. Microbiology Testing] => Array
(
[0] => Aseptic processes
[1] => Cytotoxicity testing
[2] => Medical device testing
[3] => Microbiology
[4] => Parenteral products
[5] => Sterility testing
)
[Top 7 Sources Of Microbial Contamination] => Array
(
[0] => Aseptic processes
[1] => Environmental monitoring
[2] => Medical device testing
[3] => Microbiology
[4] => Parenteral products
[5] => Sterility testing
)
[Top Biological Indicators For Each Sterilization Validation Process] => Array
(
[0] => Medical device testing
[1] => Sterility testing
)
[Sterilization By Radiation Vs. Ethylene Oxide For Medical Devices] => Array
(
[0] => EO residual testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[Water Sampling Vs. Air Sampling Methods For Environmental Monitoring] => Array
(
[0] => Environmental monitoring
[1] => Medical device testing
[2] => Microbiology
[3] => Parenteral products
[4] => Sterility testing
)
[Top 3 Sterilization Validation Methods For Medical Devices] => Array
(
[0] => Good manufacturing practices
[1] => Medical device testing
[2] => Sterility testing
)
[How To Use Dry Heat Sterilization For Depyrogenation Of Medical Devices] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
)
[Top 9 Sterilization Process Controls You Need Before Your Next Audit] => Array
(
[0] => Good manufacturing practices
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[How does the FDA classify medical devices?] => Array
(
[0] => Aseptic processes
[1] => Cosmetic products
[2] => Good manufacturing practices
[3] => Medical device testing
[4] => Microbiology
[5] => Parenteral products
)
[How To Perform Sterilization Validations For Radiation Sterilized Products] => Array
(
[0] => Good manufacturing practices
[1] => Medical device testing
[2] => Sterility testing
)
[Top 3 ISO-Approved Methods For Radiation Sterilization Dose Setting] => Array
(
[0] => Good manufacturing practices
[1] => Medical device testing
[2] => Sterility testing
)
[What Medical Devices Can Be Sterilized With Ethylene Oxide?] => Array
(
[0] => EO residual testing
[1] => Medical device testing
)
[Importance Of Medical Devices In Healthcare] => Array
(
[0] => Aseptic processes
[1] => General
[2] => Medical device testing
[3] => Microbiology
)
[What Medical Devices Aren’t Regulated By The FDA?] => Array
(
[0] => Aseptic processes
[1] => General
[2] => Medical device testing
[3] => Microbiology
)
[How To Validate Sterility In Autoclaves Vs. Radiation Sterilized Medical Products] => Array
(
[0] => General
[1] => Good manufacturing practices
[2] => Medical device testing
[3] => Sterility testing
)
[Save Start-up Time And Money Using Contract Testing Services] => Array
(
[0] => General
[1] => Good manufacturing practices
[2] => Medical device testing
[3] => Pyrogenicity testing
)
[How To Validate Steam Sterilization Processes For Medical Devices?] => Array
(
[0] => General
[1] => Good manufacturing practices
[2] => Medical device testing
[3] => Sterility testing
)
[How Do Autoclaves Sterilize Medical Devices?] => Array
(
[0] => General
[1] => Good manufacturing practices
[2] => Medical device testing
[3] => Sterility testing
)
[Contract Testing Vs. Contract Manufacturing Organizations For Medical Device Outsourcing] => Array
(
[0] => General
[1] => Good manufacturing practices
[2] => Medical device testing
[3] => Sterility testing
)
[Are Endotoxins And Lipopolysaccharides The Same?] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Pyrogenicity testing
)
[What Is The Difference Between Biological Indicators And Endotoxin Indicators?] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
)
[Top Ways To Measure Temperature For Product Sterilization] => Array
(
[0] => Good manufacturing practices
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[Top 6 Ways To Measure Humidity For Medical Device Sterilization] => Array
(
[0] => Good manufacturing practices
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[What Is Mycoplasma Sterilization?] => Array
(
[0] => Medical device testing
[1] => Sterility testing
)
[Guideline To Create Your Own Endotoxin Indicator For Regulatory Testing] => Array
(
[0] => Bacterial endotoxin testing
[1] => General
[2] => Medical device testing
[3] => Pyrogenicity testing
)
[How to depyrogenate sterile products by rinsing] => Array
(
[0] => Bacterial endotoxin testing
[1] => General
[2] => Medical device testing
[3] => Pyrogenicity testing
)
[How to depyrogenate parenteral products by filtration] => Array
(
[0] => Bacterial endotoxin testing
[1] => General
[2] => Medical device testing
[3] => Parenteral products
[4] => Pyrogenicity testing
)
[Endotoxin Removal From Sterile Products By Rinsing Vs. Filtration] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
)
[Depyrogenation Of Sterile Products By Dry Heat Vs. Filtration] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
)
[When To Use Dry Heat Vs. Rinsing For Medical Device Depyrogenation] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
)
[Depyrogenation Vs. Sterilization For Medical Devices] => Array
(
[0] => Bacterial endotoxin testing
[1] => EO residual testing
[2] => Medical device testing
[3] => Parenteral products
[4] => Pyrogenicity testing
)
[Ethylene Oxide Depyrogenation Vs. Sterilization For Medical Devices] => Array
(
[0] => Bacterial endotoxin testing
[1] => EO residual testing
[2] => Medical device testing
[3] => Parenteral products
[4] => Pyrogenicity testing
[5] => Sterility testing
)
[Dry Heat Depyrogenation vs. Sterilization For Sterile Products] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
[4] => Sterility testing
)
[Top 3 Water Sanitization Methods For Sterile Product Processing] => Array
(
[0] => Cosmetic products
[1] => Environmental monitoring
[2] => Medical device testing
[3] => Microbiology
[4] => Parenteral products
)
[What Is Vapor Phase Sterilization?] => Array
(
[0] => General
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[Vapor Phase Vs. Steam Sterilization] => Array
(
[0] => General
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[Ethylene Oxide Vs. Vapor Phase Sterilization] => Array
(
[0] => EO residual testing
[1] => General
[2] => Medical device testing
[3] => Parenteral products
[4] => Sterility testing
)
[Radiation Sterilization Vs. Vapor Sterilization] => Array
(
[0] => General
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[What Is Liquid Phase Sterilization?] => Array
(
[0] => Cosmetic products
[1] => General
[2] => Medical device testing
[3] => Parenteral products
[4] => Sterility testing
)
[Liquid Phase vs. Steam Sterilization] => Array
(
[0] => General
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[Liquid vs. Radiation Sterilization For Medical Devices] => Array
(
[0] => General
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[Liquid Vs. Vapor Phase Sterilization] => Array
(
[0] => General
[1] => Medical device testing
[2] => Parenteral products
[3] => Sterility testing
)
[Depyrogenation By Radiation Vs. Sterilization By Radiation] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Parenteral products
[3] => Pyrogenicity testing
[4] => Sterility testing
)
[What Are Sterilization Indicators & Sterilization Integrators?] => Array
(
[0] => General
[1] => Medical device testing
[2] => Sterility testing
)
[Depyrogenation And Sterilization For Medical Devices] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Pyrogenicity testing
[3] => Sterility testing
)
[Microbiology Sampling For Regulatory Testing Of Inhalable Devices] => Array
(
[0] => Good manufacturing practices
[1] => Medical device testing
[2] => Microbiology
)
[USP Guidelines On Isolator Systems] => Array
(
[0] => Environmental monitoring
[1] => Good manufacturing practices
[2] => Medical device testing
[3] => Sterility testing
)
[How to validate isolators used for medical device testing?] => Array
(
[0] => Environmental monitoring
[1] => Medical device testing
[2] => Sterility testing
)
[Direct Contact Vs. Elution Cytotoxicity Testing] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
[2] => Parenteral products
)
[Agar Diffusion Vs. Direct Contact Cytotoxicity Testing] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
[2] => Parenteral products
)
[Elution Vs. Agar Diffusion Cytotoxicity Testing] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
[2] => Parenteral products
)
[Cytotoxicity Testing Vs. Physiochemical Testing For Medical-Grade Plastics] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
[2] => Parenteral products
)
[Is Sensitization Testing Needed For Regulatory Approval Of Medical Devices?] => Array
(
[0] => Cytotoxicity testing
[1] => General
[2] => Medical device testing
)
[Ethylene Oxide Residuals Simulated-Use Extraction Measuring Methods] => Array
(
[0] => EO residual testing
[1] => General
[2] => Medical device testing
)
[Ethylene Oxide Residuals Exhaustive Extraction Measuring Methods] => Array
(
[0] => EO residual testing
[1] => General
[2] => Medical device testing
)
[In-Vitro USP 87 Vs. In-Vivo USP 88 Cytotoxicity Testing] => Array
(
[0] => Cytotoxicity testing
[1] => General
[2] => Medical device testing
[3] => Parenteral products
)
[How To Prepare Your Samples For Ethylene Oxide Residuals Testing] => Array
(
[0] => EO residual testing
[1] => General
[2] => Medical device testing
)
[How Do You Select Biocompatibility Tests For Medical Devices & Implants?] => Array
(
[0] => General
[1] => Medical device testing
)
[How Much Does Medical Device Development Cost?] => Array
(
[0] => General
[1] => Good manufacturing practices
[2] => Medical device testing
)
[How Do You Perform Endotoxin Tests And Pyrogen Tests?] => Array
(
[0] => Bacterial endotoxin testing
[1] => Medical device testing
[2] => Pyrogenicity testing
)
[USP 87 In-Vitro Cytotoxicity Testing] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
[2] => Parenteral products
)
[USP 88 In-Vivo Cytotoxicity Testing] => Array
(
[0] => Cytotoxicity testing
[1] => Medical device testing
[2] => Parenteral products
)
[Which Is The Best Sterilization Method For Your Medical Device?] => Array
(
[0] => Medical device testing
[1] => Sterility testing
)
[How is EtO residuals testing performed?] => Array
(
[0] => EO residual testing
[1] => Medical device testing
)
[Microbial Aerosol Challenge Testing vs. Bioburden Testing] => Array
(
[0] => Bioburden testing
[1] => Medical device testing
[2] => Package integrity testing
[3] => Parenteral products
)
[Microbial Aerosol Challenge Testing vs. Microbiology Testing] => Array
(
[0] => Medical device testing
[1] => Microbiology
[2] => Package integrity testing
[3] => Parenteral products
)
[What is electron beam sterilization?] => Array
(
[0] => Medical device testing
[1] => Sterility testing
)
[Electron Beam vs. Gamma Radiation Sterilization] => Array
(
[0] => Medical device testing
[1] => Sterility testing
)
[What Are Restricted Access Barrier Systems (RABS)?] => Array
(
[0] => Environmental monitoring
[1] => Medical device testing
[2] => Sterility testing
)
[Isolators Vs. Restricted Access Barrier Systems] => Array
(
[0] => Environmental monitoring
[1] => Medical device testing
[2] => Sterility testing
)
[How To Calculate Tolerable Contact Limits For Ethylene Oxide] => Array
(
[0] => EO residual testing
[1] => Medical device testing
[2] => Sterility testing
)
[Key Differences Between USP 1115, USP 1116 and USP 1211] => Array
(
[0] => Bioburden testing
[1] => Good manufacturing practices
[2] => Medical device testing
[3] => Sterility testing
)
[Tolerable Exposure Limits For Ethylene Oxide Sterilized Medical Devices] => Array
(
[0] => EO residual testing
[1] => Medical device testing
[2] => Sterility testing
)
[How To Calculate Allowable Limits For Ethylene Oxide Sterilization] => Array
(
[0] => EO residual testing
[1] => Medical device testing
[2] => Sterility testing
)
[The Benefits of Outsourcing Medical Device Product Testing] => Array
(
[0] => General
)
[Accelerating Time to Market By Streamlining Medical Device Testing] => Array
(
[0] => General
)
[How Comprehensive Product Testing Expertise Reduces Risk for Medtech Manufacturers] => Array
(
[0] => General
)
)