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• Medical Devices
  • Extractables & Leachables for Medical Devices (Chemical Characterization)
    • Material Characterization Screens of Raw Materials
    • Physicochemical USP Plastics Tests
  • Facility & Process Validation
    • Disinfection Efficacy Studies
    • Environmental Monitoring Supplies – Air & Water
    • Environmental Monitoring Tests – Air & Water
    • Filter Sterilization Validations
    • Forced Degradation
    • Material Characterization Screens of Raw Materials
    • Residual Manufacturing Materials
    • Water System Validations & Monitoring
  • Medical Device Antimicrobials and Disinfectants
    • Antimicrobial Preservative Effectiveness
    • Cleaning and Disinfectant Validation
    • Disinfectant Efficacy
    • MIC/MBC
    • Microbial Ingress
    • Time-Kill Evaluations
    • Zone of Inhibition
  • Medical Device Biocompatibility & Toxicology
    • Cytotoxicity
    • Genotoxicity
    • Hemocompatibility
    • Implantation with Histopathology Tests
    • Irritation
    • ISO 18562: Biocompatibility Evaluation of Breathing Gas Pathway Devices
    • Physicochemical USP Plastics Tests
    • Risk Assessments
    • Sensitization
    • Subacute & Subchronic Toxicity
    • Systemic Toxicity Test
  • Medical Device General Considerations
  • Medical Device Method Development
  • Packaging Solutions
    • Accelerated & Real-Time Aging
    • Container Closure Integrity – Dye Immersion & Bacterial Immersion
    • Container Closure Integrity – Mass Extraction
    • Microbial Barrier Testing
    • Packaging Integrity & Strength Test
    • Packaging Shelf Life Studies
    • Transportation and Distribution Performance
  • Personal Protective Equipment (PPE) Reprocessing
  • Protective Barriers
    • Antimicrobial Efficacy Studies
    • Bacterial & Viral Filtration Efficiency (BFE/VFE)
    • Barrier Face Coverings Test
    • Fit Capability Testing
    • Flammability Test
    • Glove Testing
    • Hydrostatic Pressure Test
    • Microbial Cleanliness for Face Masks
    • Particle Filtration Efficiency (PFE)
    • Respirator Pre-Submission Tests – NIOSH
    • Spray Impact
    • Surgical Face Masks and General-Use Masks – ASTM F2100 & EN 14683
    • Surgical/Isolation Gowns and Drapes – AAMI PB70, ASTM F2407/F3352, & EN 13795
    • Synthetic Blood Penetration for Liquid Barriers
    • Tensile and Tear Resistance Tests for Fabrics
    • Viral Penetration Test
  • Reusable Medical Device Processing
    • Cleaning Validation – Reusable Devices
    • Disinfection Validation Testing for Reusable Devices
    • End-of-Life Testing
    • Human Factors Testing – Reprocessing Instructions
    • Scope Processing Validations for Reusable Devices
    • Sterilization Validation – Reuse Device
  • Sterility Assurance
    • Antibiotic Potency Test
    • Antimicrobial Preservative Effectiveness
    • Bacterial Endotoxins Test
    • Biological Indicator – Population Verification
    • Biological Indicator – Rapid Sterility Testing
    • Biological Indicator – Sterility Testing
    • EO Sterilant Residual Tests
    • Method Suitability (Bacteriostasis/Fungistasis)
    • Microbial Identifications
    • Particulate Matter
    • Product Bioburden – Medical Device
    • Product Sterility – Cleanroom
    • Product Sterility – Isolator
    • Product Sterility – Rapid
    • Radiation Quarterly Dose Audits (QDAs)
    • Recombinant Bacterial Endotoxin Testing
    • Standard Plate Counts
  • Sterilization Validations
    • Clinical Batch Release
    • Contract Sterilization – Sterigenics
    • D-Value Determination Studies
    • Filter Sterilization Validations
    • Product Inoculations
    • Sterilization Exposure Cycles
    • Sterilization Relative Resistance
    • Sterilization Supplies (BIs, PCDs, & TestPacks)
    • Sterilization Validation – Ethylene Oxide (EO)
    • Sterilization Validation – Hydrogen Peroxide
    • Sterilization Validation – Radiation
    • Sterilization Validation – Reuse Device
• Pharmaceutical
  • Chemistry Testing
    • Compendial Testing
    • Drug Assay (Active Ingredients and Dosage Forms)
    • Excipient Testing
    • Wet Chemistry Capabilities
  • Extractables & Leachables for Pharmaceuticals
    • Compounds Screener Database
    • Inhalables OINDP
    • Injectables & Parenterals
    • Label Migration Studies
    • Liquid Oral Dosage Forms
    • Manufacturing Systems
    • Material Characterization Screens of Raw Materials
    • Ophthalmics
    • Pharmaceutical General Considerations
    • Physicochemical USP Plastics Tests
    • Topical Dosage Forms
  • Facility & Process Validation
    • Disinfection Efficacy Studies
    • Environmental Monitoring Supplies – Air & Water
    • Environmental Monitoring Tests – Air & Water
    • Filter Sterilization Validations
    • Water System Validations & Monitoring
    • Water Testing
    • Wet Chemistry Capabilities
  • Impurities in Drug Components & API
  • Packaging and Stability Solutions
    • Accelerated & Real-Time Aging
    • Container Closure Integrity – Dye Immersion & Bacterial Immersion
    • Container Closure Integrity – Mass Extraction
    • Microbial Barrier Testing
    • Packaging Integrity & Strength Test
    • Packaging Shelf Life Studies
    • Stability Studies – Pharmaceutical
    • Transportation and Distribution Performance
    • Wet Chemistry Capabilities
  • Pharmaceutical Antimicrobials and Disinfectants
    • Antimicrobial Preservative Effectiveness
    • Disinfectant Efficacy
    • MIC/MBC
    • Microbial Ingress
    • Time-Kill Evaluations
    • Zone of Inhibition
  • Pharmaceutical Biocompatibility & Toxicology
    • Cytotoxicity
    • Genotoxicity
    • Physicochemical USP Plastics Tests
    • Risk Assessments
    • Systemic Toxicity Test
  • Pharmaceutical Method Development
    • Forced Degradation
  • Sterility Assurance
    • Antibiotic Potency Test
    • Antimicrobial Preservative Effectiveness
    • Bacterial Endotoxins Test
    • Impurities Identification
    • Method Suitability (Bacteriostasis/Fungistasis)
    • Microbial Identifications
    • Microbiological Examination of Nonsterile Products
    • Mycoplasma Testing – PCR & Traditional
    • Particulate Matter
    • Product Sterility – Cleanroom
    • Product Sterility – Isolator
    • Product Sterility – Rapid
    • Radiation Quarterly Dose Audits (QDAs)
    • Recombinant Bacterial Endotoxin Testing
    • Zone of Inhibition
  • Sterilization Validations
    • Contract Sterilization – Sterigenics
    • Filter Sterilization Validations
• Tissue Testing
  • Facility & Process Validation
    • Disinfection Efficacy Studies
    • Environmental Monitoring Supplies – Air & Water
    • Environmental Monitoring Tests – Air & Water
    • Water System Validations & Monitoring
  • Packaging Solutions
    • Accelerated & Real-Time Aging
    • Packaging Integrity & Strength Test
    • Packaging Shelf Life Studies
  • Sterility Assurance
    • Microbial Identifications
    • Product Bioburden – Tissue
    • Product Sterility – Cleanroom
    • Radiation Quarterly Dose Audits (QDAs)
    • Recombinant Bacterial Endotoxin Testing
    • Standard Plate Counts
  • Sterilization Validations
    • Contract Sterilization – Sterigenics
    • D-Value Determination Studies
    • Product Inoculations
    • Sterilization Validation – Hydrogen Peroxide
    • Sterilization Validation – Radiation

• Medical Devices (13)
  • Extractables & Leachables for Medical Devices (Chemical Characterization) (2)
    • Material Characterization Screens of Raw Materials
    • Physicochemical USP Plastics Tests
  • Facility & Process Validation (8)
    • Disinfection Efficacy Studies
    • Environmental Monitoring Supplies – Air & Water
    • Environmental Monitoring Tests – Air & Water
    • Filter Sterilization Validations
    • Forced Degradation
    • Material Characterization Screens of Raw Materials
    • Residual Manufacturing Materials
    • Water System Validations & Monitoring
  • Medical Device Antimicrobials and Disinfectants (7)
    • Antimicrobial Preservative Effectiveness
    • Cleaning and Disinfectant Validation
    • Disinfectant Efficacy
    • MIC/MBC
    • Microbial Ingress
    • Time-Kill Evaluations
    • Zone of Inhibition
  • Medical Device Biocompatibility & Toxicology (11)
    • Cytotoxicity
    • Genotoxicity
    • Hemocompatibility
    • Implantation with Histopathology Tests
    • Irritation
    • ISO 18562: Biocompatibility Evaluation of Breathing Gas Pathway Devices
    • Physicochemical USP Plastics Tests
    • Risk Assessments
    • Sensitization
    • Subacute & Subchronic Toxicity
    • Systemic Toxicity Test
  • Medical Device General Considerations
  • Medical Device Method Development
  • Medical Devices
  • Packaging Solutions (7)
    • Accelerated & Real-Time Aging
    • Container Closure Integrity – Dye Immersion & Bacterial Immersion
    • Container Closure Integrity – Mass Extraction
    • Microbial Barrier Testing
    • Packaging Integrity & Strength Test
    • Packaging Shelf Life Studies
    • Transportation and Distribution Performance
  • Personal Protective Equipment (PPE) Reprocessing
  • Protective Barriers (16)
    • Antimicrobial Efficacy Studies
    • Bacterial & Viral Filtration Efficiency (BFE/VFE)
    • Barrier Face Coverings Test
    • Fit Capability Testing
    • Flammability Test
    • Glove Testing
    • Hydrostatic Pressure Test
    • Microbial Cleanliness for Face Masks
    • Particle Filtration Efficiency (PFE)
    • Respirator Pre-Submission Tests – NIOSH
    • Spray Impact
    • Surgical Face Masks and General-Use Masks – ASTM F2100 & EN 14683
    • Surgical/Isolation Gowns and Drapes – AAMI PB70, ASTM F2407/F3352, & EN 13795
    • Synthetic Blood Penetration for Liquid Barriers
    • Tensile and Tear Resistance Tests for Fabrics
    • Viral Penetration Test
  • Reusable Medical Device Processing (6)
    • Cleaning Validation – Reusable Devices
    • Disinfection Validation Testing for Reusable Devices
    • End-of-Life Testing
    • Human Factors Testing – Reprocessing Instructions
    • Scope Processing Validations for Reusable Devices
    • Sterilization Validation – Reuse Device
  • Sterility Assurance (17)
    • Antibiotic Potency Test
    • Antimicrobial Preservative Effectiveness
    • Bacterial Endotoxins Test
    • Biological Indicator – Population Verification
    • Biological Indicator – Rapid Sterility Testing
    • Biological Indicator – Sterility Testing
    • EO Sterilant Residual Tests
    • Method Suitability (Bacteriostasis/Fungistasis)
    • Microbial Identifications
    • Particulate Matter
    • Product Bioburden – Medical Device
    • Product Sterility – Cleanroom
    • Product Sterility – Isolator
    • Product Sterility – Rapid
    • Radiation Quarterly Dose Audits (QDAs)
    • Recombinant Bacterial Endotoxin Testing
    • Standard Plate Counts
  • Sterilization Validations (12)
    • Clinical Batch Release
    • Contract Sterilization – Sterigenics
    • D-Value Determination Studies
    • Filter Sterilization Validations
    • Product Inoculations
    • Sterilization Exposure Cycles
    • Sterilization Relative Resistance
    • Sterilization Supplies (BIs, PCDs, & TestPacks)
    • Sterilization Validation – Ethylene Oxide (EO)
    • Sterilization Validation – Hydrogen Peroxide
    • Sterilization Validation – Radiation
    • Sterilization Validation – Reuse Device
• Pharmaceutical (11)
  • Chemistry Testing (4)
    • Compendial Testing
    • Drug Assay (Active Ingredients and Dosage Forms)
    • Excipient Testing
    • Wet Chemistry Capabilities
  • Extractables & Leachables for Pharmaceuticals (11)
    • Compounds Screener Database
    • Inhalables OINDP
    • Injectables & Parenterals
    • Label Migration Studies
    • Liquid Oral Dosage Forms
    • Manufacturing Systems
    • Material Characterization Screens of Raw Materials
    • Ophthalmics
    • Pharmaceutical General Considerations
    • Physicochemical USP Plastics Tests
    • Topical Dosage Forms
  • Facility & Process Validation (7)
    • Disinfection Efficacy Studies
    • Environmental Monitoring Supplies – Air & Water
    • Environmental Monitoring Tests – Air & Water
    • Filter Sterilization Validations
    • Water System Validations & Monitoring
    • Water Testing
    • Wet Chemistry Capabilities
  • Impurities in Drug Components & API
  • Packaging and Stability Solutions (9)
    • Accelerated & Real-Time Aging
    • Container Closure Integrity – Dye Immersion & Bacterial Immersion
    • Container Closure Integrity – Mass Extraction
    • Microbial Barrier Testing
    • Packaging Integrity & Strength Test
    • Packaging Shelf Life Studies
    • Stability Studies – Pharmaceutical
    • Transportation and Distribution Performance
    • Wet Chemistry Capabilities
  • Pharmaceutical Antimicrobials and Disinfectants (6)
    • Antimicrobial Preservative Effectiveness
    • Disinfectant Efficacy
    • MIC/MBC
    • Microbial Ingress
    • Time-Kill Evaluations
    • Zone of Inhibition
  • Pharmaceutical Biocompatibility & Toxicology (5)
    • Cytotoxicity
    • Genotoxicity
    • Physicochemical USP Plastics Tests
    • Risk Assessments
    • Systemic Toxicity Test
  • Pharmaceutical Method Development (1)
    • Forced Degradation
  • Sterility Assurance (14)
    • Antibiotic Potency Test
    • Antimicrobial Preservative Effectiveness
    • Bacterial Endotoxins Test
    • Impurities Identification
    • Method Suitability (Bacteriostasis/Fungistasis)
    • Microbial Identifications
    • Microbiological Examination of Nonsterile Products
    • Mycoplasma Testing – PCR & Traditional
    • Particulate Matter
    • Product Sterility – Cleanroom
    • Product Sterility – Isolator
    • Product Sterility – Rapid
    • Radiation Quarterly Dose Audits (QDAs)
    • Recombinant Bacterial Endotoxin Testing
    • Zone of Inhibition
  • Sterilization Validations (2)
    • Contract Sterilization – Sterigenics
    • Filter Sterilization Validations
• Tissue Testing (4)
  • Facility & Process Validation (4)
    • Disinfection Efficacy Studies
    • Environmental Monitoring Supplies – Air & Water
    • Environmental Monitoring Tests – Air & Water
    • Water System Validations & Monitoring
  • Packaging Solutions (3)
    • Accelerated & Real-Time Aging
    • Packaging Integrity & Strength Test
    • Packaging Shelf Life Studies
  • Sterility Assurance (6)
    • Microbial Identifications
    • Product Bioburden – Tissue
    • Product Sterility – Cleanroom
    • Radiation Quarterly Dose Audits (QDAs)
    • Recombinant Bacterial Endotoxin Testing
    • Standard Plate Counts
  • Sterilization Validations (5)
    • Contract Sterilization – Sterigenics
    • D-Value Determination Studies
    • Product Inoculations
    • Sterilization Validation – Hydrogen Peroxide
    • Sterilization Validation – Radiation