InrexTest
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What we do

InrexTest facilitates and coordinates pharmaceutical and medical device studies through our team of internal experts coupled with top quality labs supporting preclinical and clinical testing at every stage of development. At InrexTest, we understand customers’ priorities. We utilize our technical expertise to design and customize individualized research projects based on client inputs. We qualify and audit testing facilities that are best suited to conduct your research. Our highly competent staff oversees the complete execution of the project and delivery of signed reports to the client.

InrexTest demands the highest standards of quality and accuracy along with the timely completion of studies at the best possible price. Data packages are 100% reviewed for their accuracyand completeness for the regulatory submission anticipated.

InrexTest provides a fullsuite of testing services and comprehensive guidance, from establishing the testing protocol through test completion and regulatory submission; assisting you from initial product development until your product reaches the market.

  • 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