InrexTest
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The InrexTest Advantage

InrexTest works with experienced partner laboratories and clinics worldwide to provide the highest quality and best pricing available in the industry. Since many of our partner facilities are located in India, we have an office in Pune to support legal, regulatory, and project management services. By maintaining these functions both in Pune and in our home office in New York, we provide assurance of quick turnaround, quality results, and highly competitive pricing.

As your agent, InrexTest works for you with our partner laboratories and clinics to assure your testing needs are understood and executed properly no matter what your filing or quality standard requirements. We qualify and select the best partner labs or clinics to meet quality, timeliness, and financial goals. We inspect and monitor to assure that GLP, GCP, GMP, ISO, CAPA or CLIA standards are met.

Over the course of your project, our highly experienced project management team monitors the work and documentation.

We facilitate the logistics of sample transport and assure that the chain of custody is intact. We also inspect to assure all materials used for testing are appropriate and that all IQ/OQ are performed and documented as required.

At InrexTest, we take pride in providing a service that we believe is second to none in the industry. Call us to discuss your next project.

  • Project Management
    • Study Plan and Design
    • Lab Selection
    • Lab Auditing
    • Meeting Coordination
    • Study Monitoring
    • Regulatory Consulting
  • Analytical Development
    • Preformulation Studies
    • Formulation Development
    • Analytical Development
    • Stability Studies
    • Storage Conditions
    • Pharmacopoeial Testings
    • Raw Materials and Excipients Analysis
  • List of Validated Bioanalytical Methods
  • Preclinical Research
    • NCE Screening
    • ADME / DMPK studies
    • Toxicology Testing
    • In Vivo Toxicology Test Categories
    • Available Species
    • Available Models
  • Clinical Research
    • Drug Formulation Trials
    • Device Trials
    • First in Human - Phase I
    • Pharmacovigilance
    • Clinical Data Management (CDM)
    • Medical writing and Translation
    • Regulatory Affairs
  • Microbiology and Sterilization
    • MIC Testing
    • USP Microbial Testing
    • Bioburden Testing
    • Antimicrobial Assay
    • Antimicrobial Efficacy
    • Cleaning Validation
    • EO Sterilization
  • Medical Device Testing
    • Biocompatibility- ISO 10993
  • Our Partners
    • ASTM - D551 Biodegradable Testing
© InrexTest - 2012 | Powered by Infinity
  • What we do
  • The InrexTest Advantage
  • Management
  • Vision & Mission
  • FAQ's
Project Management
  • Study Plan and Design
  • Lab Selection
  • Lab Auditing
  • Meeting Coordination
  • Study Monitoring
  • Regulatory Consulting
Analytical Development
  • Preformulation Studies
  • Formulation Development
  • Analytical Development
  • Stability Studies
  • Storage Conditions
  • Pharmacopoeial Testings
  • Raw Materials and Excipients Analysis
  • List of Validated Bioanalytical Methods
Preclinical Research
  • NCE Screening
  • ADME / DMPK studies
  • Toxicology Testing
  • In Vivo Toxicology Test Categories
  • Available Species
  • Available Models
Clinical Research
  • Drug Formulation Trials
  • Device Trials
  • First in Human - Phase I
  • Pharmacovigilance
  • Clinical Data Management (CDM)
  • Medical writing and Translation
  • Regulatory Affairs
Microbiology and Sterilization
  • MIC Testing
  • USP Microbial Testing
  • Bioburden Testing
  • Antimicrobial Assay
  • Antimicrobial Efficacy
  • Cleaning Validation
  • EO Sterilization
Medical Device Testing
  • Biocompatibility- ISO 10993