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      Expert In Silico toxicology support delivering a wide range of reports with proven regulatory acceptance.
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      Target safety assessment service for detailed insights into potential toxicological risks associated with drug targets.
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      Advanced Translational Safety Solution enabling data alignment and review and visualizations.
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      Services delivering a detailed, expert-led S1B Weight of Evidence (WoE) assessment accelerating your development timeline.
      Key Insights from the Leadscope Consultants User Group Meeting
      Insights from the Leadscope Consultants User Group Meeting
      Leadscope’s Key Features Supporting Drug Discovery and Development.

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      ClimbNEW
      Capture pre-clinical in vivo data from any therapeutic area into the cloud to accelerate studies.
      Provantis
      Market leading solution for preclinical GLP study management.
      Morphit
      Simplifies the process of capturing, analyzing, and reporting data for faster discovery research.
      Pristima
      Xybion Legacy study management software.
      BioRails
      Discovery solution optimizing bioanalysis workflows, accelerating in vitro ADME/DMPK studies and in vivo PK studies.
      Comet Assay IV
      Image analysis system for consistent and reliable comet assay scoring.
      Logbook
      Digitalization software enabling researchers to move away from paper-based systems.
      NOTOCORD-hem
      Software for advanced acquisition, analysis, and custom reporting of physiological signals.
      Cyto Study Manager
      Comprehensive Genetox assay management on one platform accelerating workflows and reducing costs.
      Kits ecommerce dropdown
      Climb’s Innovation Continues at Instem
      Advancing Non-GLP In Vivo Research with Speed, Flexibility, and Scientific Focus.

      Read Press Release

      SEND Advantage Services
      Services providing accelerated submission-ready SEND conversions, consultation, and verification.
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      Electronic quality management system for regulatory compliance processes.
      Submit
      Quickly create and manage high quality submission-ready SEND packages with a single suite of tools.
      Compliance BuilderNEW
      Audit trail and data integrity solution for scientific systems and files.
      SEND dataset 5-step blog
      A 5-Step SEND Dataset Checklist to Ensure Data Compliance
      It’s important to consider SEND guidelines throughout the process, not only before submission, to prevent costly surprises.

      Download Now

      Matrix Gemini LIMSNEW
      Configurable LIMS covering data collection, storage, and reporting while meeting global compliance and quality standards.
      choosing the right LIMS
      How to Select the Next Generation of Digital LIMS
      The Matrix Gemini LIMS white paper outlines four key considerations: performance, compliance, flexibility, and cost efficiency, to help laboratories choose the next generation of digital LIMS.

      Read Now

      Accel
      A turnkey, validated, and easy-to-use clinical analytics platform for all-sized biostats teams.
      Clinical Trial Transparency (CTT) Services
      Future-proof data and document sharing with de-identification and transparency strategizing services.
      Aspire
      Cloud-based SCE designed for large biostats teams looking to scale, automate, and future-proof workflows.
      Custom SCENEW
      A suite of services and technologies designed to build a tailored clinical analytics platform.
      Blur
      SaaS platform for de-identifying data and documents from clinical trials, removing risk and ensuring patient privacy.
      Kits ecommerce dropdown
      How to Build the Right SCE for Your Team
      This white paper explores the essential components of an effective SCE in clinical settings.

      Download Whitepaper

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      Matrix Gemini LIMS delivers a flexible, configurable, and future-proof solution for laboratories of all sizes, helping users manage samples, data, and workflows efficiently while ensuring full regulatory compliance.

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      Support GxP workflows from discovery to QC.
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      Safeguard consumers with traceable testing workflows.
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      Improve patient outcomes with reliable lab data.
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      Streamline case management from receipt to report.
      Radiopharmacy
      Manage short half-life products with full traceability.
      Water & Environmental
      Ensure compliance with environmental testing standards.
      Manufacturing
      Connect QC labs to production line decisions.
      Medical Device
      Meet strict regulatory and quality requirements.
      Petrochemical
      Optimize fuel, oil, and gas testing operations.
      Veterinary
      Enhance animal health diagnostics and reporting.
      Kits ecommerce dropdown
      Matrix Gemini LIMS Fact Sheet
      Matrix Gemini LIMS delivers a flexible, configurable, and future-proof solution for laboratories of all sizes, helping users manage samples, data, and workflows efficiently while ensuring full regulatory compliance.

      Download Now

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      Explore our available training courses provided by Instem.
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      Watch on-demand sessions exploring emerging trends, product innovations, and best practices in life sciences R&D.
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      Read the latest blogs and gain industry insights from Instem’s deep bench of SMEs.
      White Papers
      In-depth analyses and technical papers providing guidance on regulatory compliance, data management, and research optimization.
      Provantis SRI case study
      The Journey of a Molecule: Why Integration Matters in Modern Drug Development
      Follow the journey from early research to regulatory submission and learn how Instem helps teams work more efficiently, reduce risk, and deliver safer, more effective therapies to patients faster.

      Download Infographic

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    3 2
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      Contact Us
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      Careers
      Explore opportunities to join Instem and help shape the future of research and discovery worldwide.
      Kits ecommerce dropdown
      Climb’s Innovation Continues at Instem
      Advancing Non-GLP In Vivo Research with Speed, Flexibility, and Scientific Focus.

      Read Now

  • Solutions NEW
    3 2
      In Silico & Data Insights
      Study Management
      Regulatory Submission
      Lab Execution
      Clinical Trial Analytics and Transparency
      Leadscope Model Applier
      Accelerating R&D by delivering accurate predictions for wide-ranging toxicological endpoints, driven by regulatory guidelines.
      Predict
      Expert In Silico toxicology support delivering a wide range of reports with proven regulatory acceptance.
      KnowledgeScan
      Target safety assessment service for detailed insights into potential toxicological risks associated with drug targets.
      Centrus
      Advanced Translational Safety Solution enabling data alignment and review and visualizations.
      Advance
      Services delivering a detailed, expert-led S1B Weight of Evidence (WoE) assessment accelerating your development timeline.
      Key Insights from the Leadscope Consultants User Group Meeting
      Insights from the Leadscope Consultants User Group Meeting
      Leadscope’s Key Features Supporting Drug Discovery and Development.

      Read Now

      ClimbNEW
      Capture pre-clinical in vivo data from any therapeutic area into the cloud to accelerate studies.
      Provantis
      Market leading solution for preclinical GLP study management.
      Morphit
      Simplifies the process of capturing, analyzing, and reporting data for faster discovery research.
      Pristima
      Xybion Legacy study management software.
      BioRails
      Discovery solution optimizing bioanalysis workflows, accelerating in vitro ADME/DMPK studies and in vivo PK studies.
      Comet Assay IV
      Image analysis system for consistent and reliable comet assay scoring.
      Logbook
      Digitalization software enabling researchers to move away from paper-based systems.
      NOTOCORD-hem
      Software for advanced acquisition, analysis, and custom reporting of physiological signals.
      Cyto Study Manager
      Comprehensive Genetox assay management on one platform accelerating workflows and reducing costs.
      Kits ecommerce dropdown
      Climb’s Innovation Continues at Instem
      Advancing Non-GLP In Vivo Research with Speed, Flexibility, and Scientific Focus.

      Read Press Release

      SEND Advantage Services
      Services providing accelerated submission-ready SEND conversions, consultation, and verification.
      Quality System Management (eQCM)NEW
      Electronic quality management system for regulatory compliance processes.
      Submit
      Quickly create and manage high quality submission-ready SEND packages with a single suite of tools.
      Compliance BuilderNEW
      Audit trail and data integrity solution for scientific systems and files.
      SEND dataset 5-step blog
      A 5-Step SEND Dataset Checklist to Ensure Data Compliance
      It’s important to consider SEND guidelines throughout the process, not only before submission, to prevent costly surprises.

      Download Now

      Matrix Gemini LIMSNEW
      Configurable LIMS covering data collection, storage, and reporting while meeting global compliance and quality standards.
      choosing the right LIMS
      How to Select the Next Generation of Digital LIMS
      The Matrix Gemini LIMS white paper outlines four key considerations: performance, compliance, flexibility, and cost efficiency, to help laboratories choose the next generation of digital LIMS.

      Read Now

      Accel
      A turnkey, validated, and easy-to-use clinical analytics platform for all-sized biostats teams.
      Clinical Trial Transparency (CTT) Services
      Future-proof data and document sharing with de-identification and transparency strategizing services.
      Aspire
      Cloud-based SCE designed for large biostats teams looking to scale, automate, and future-proof workflows.
      Custom SCENEW
      A suite of services and technologies designed to build a tailored clinical analytics platform.
      Blur
      SaaS platform for de-identifying data and documents from clinical trials, removing risk and ensuring patient privacy.
      Kits ecommerce dropdown
      How to Build the Right SCE for Your Team
      This white paper explores the essential components of an effective SCE in clinical settings.

      Download Whitepaper

  • Applications
    3 2
      By Role
      LIMS Applications
      Lab Operations
      Lab Managers and Facility Supervisors rely on connected systems to streamline workflows and ensure compliance.
      Data Managers
      IT and Regulatory Leads safeguard data quality, submissions, and traceability across global research programs.
      Safety Professionals
      Toxicologists, Pathologists, and Safety Directors drive decisions with integrated tools and predictive insights.
      Biostats Professionals
      Biostatisticians and Data Science Leads ensure valid, compliant analysis across preclinical and clinical studies.
      Study Leaders
      Study Directors and Program Managers coordinate study planning, execution, and reporting across disciplines.
      Kits ecommerce dropdown
      Matrix Gemini LIMS Fact Sheet
      Matrix Gemini LIMS delivers a flexible, configurable, and future-proof solution for laboratories of all sizes, helping users manage samples, data, and workflows efficiently while ensuring full regulatory compliance.

      Download Now

      Biobank Management
      Track samples, storage, and chain of custody.
      Food & Beverage
      Deliver quality, consistency, and regulatory confidence.
      Materials, Metals & Mining
      Accelerate assay results and sample throughput.
      Nuclear & Radiochemical
      Handle sensitive testing with precision and safety.
      Pharmaceutical
      Support GxP workflows from discovery to QC.
      Contract Laboratory
      Manage clients, projects, and billing seamlessly.
      Food Safety
      Safeguard consumers with traceable testing workflows.
      Medical & Healthcare
      Improve patient outcomes with reliable lab data.
      Pathology
      Streamline case management from receipt to report.
      Radiopharmacy
      Manage short half-life products with full traceability.
      Water & Environmental
      Ensure compliance with environmental testing standards.
      Manufacturing
      Connect QC labs to production line decisions.
      Medical Device
      Meet strict regulatory and quality requirements.
      Petrochemical
      Optimize fuel, oil, and gas testing operations.
      Veterinary
      Enhance animal health diagnostics and reporting.
      Kits ecommerce dropdown
      Matrix Gemini LIMS Fact Sheet
      Matrix Gemini LIMS delivers a flexible, configurable, and future-proof solution for laboratories of all sizes, helping users manage samples, data, and workflows efficiently while ensuring full regulatory compliance.

      Download Now

  • Resources
    3 2
      Resources
      All Resources
      Check out the latest resources including whitepapers, flyers, webinars and more.
      Case Studies
      Discover how leading organizations are accelerating their research using Instem’s solutions and services.
      Training
      Explore our available training courses provided by Instem.
      Fact Sheets
      Concise product summaries highlighting key features, benefits, and technical specifications.
      Webinars
      Watch on-demand sessions exploring emerging trends, product innovations, and best practices in life sciences R&D.
      Blog
      Read the latest blogs and gain industry insights from Instem’s deep bench of SMEs.
      White Papers
      In-depth analyses and technical papers providing guidance on regulatory compliance, data management, and research optimization.
      Provantis SRI case study
      The Journey of a Molecule: Why Integration Matters in Modern Drug Development
      Follow the journey from early research to regulatory submission and learn how Instem helps teams work more efficiently, reduce risk, and deliver safer, more effective therapies to patients faster.

      Download Infographic

  • Company
    3 2
      Company
      About Us
      Learn more about Instem’s history, culture, and mission to enable smarter, faster decisions in life sciences R&D.
      Events
      Meet the team at upcoming conferences and industry gatherings around the world.
      Leadership Team
      Meet the leaders guiding Instem’s strategy and driving innovation across our global organization.
      Company News
      Stay up to date with the latest announcements, product releases, and corporate developments from Instem.
      Contact Us
      Get in touch with our team for product information, support, or partnership opportunities.
      Careers
      Explore opportunities to join Instem and help shape the future of research and discovery worldwide.
      Kits ecommerce dropdown
      Climb’s Innovation Continues at Instem
      Advancing Non-GLP In Vivo Research with Speed, Flexibility, and Scientific Focus.

      Read Now

Contact Us
Book a Demo
  • Solutions
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      • Pristima
      • Logbook
      • Provantis
      • Biorails
      • NOTOCORD-hem
      • Morphit
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      • Cyto Study Manager
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Why Define-XML files give me the Happy Mondays

Why Define-XML files give me the Happy Mondays

by Marc Ellison | Sep 15, 2021 | Regulatory Submission, SEND, Sensible SEND

During my formative years, there was a band from the north of England, not far from where I was growing up, called the Happy Mondays. Probably the most notable thing about them was one bandmember called ‘Bez’. His contribution was somewhere between cheerleading and...
Can SEND datasets be fully compliant…but still wrong?

Can SEND datasets be fully compliant…but still wrong?

by Marc Ellison | Sep 1, 2021 | Regulatory Submission, SEND, Sensible SEND

In a recent post, we discussed how there’s quite a bit of emphasis at the moment on ensuring SEND datasets are compliant with the SEND Standard. Obviously, the main driver here is the activation of the FDA’s technical rejection criteria, which will result in the...
Did you see the recent paper from the JPMA SEND Taskforce Team?

Did you see the recent paper from the JPMA SEND Taskforce Team?

by Marc Ellison | Aug 18, 2021 | Regulatory Submission, SEND, Sensible SEND

Okay, first – some context… Without the FDA requiring SEND datasets, we would not have seen the industry-wide adoption and implementation of the standard. The change made by the industry, continues to fascinate me, in terms of both speed and scale. This drive for...
There’s a theme developing here

There’s a theme developing here

by Marc Ellison | Aug 4, 2021 | Regulatory Submission, SEND, Sensible SEND

Human beings have an inherent ability to see patterns in everyday objects, like recognizing shapes and faces in clouds. While that might seem ridiculous, pattern recognition is vital for us. Without it, we would not be able to do things as varied as being able to...
How to avoid rejection

How to avoid rejection

by Marc Ellison | Jul 21, 2021 | Regulatory Submission, SEND, Sensible SEND

It’s a basic human need: We want our work accepted and valued. Nobody wants to see their work rejected. It’s so obvious, it almost goes without saying. Worse still would be being rejected by a cold, heartless automated computerized system. That would be soul...
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Life Science Software – Drug Research & Development
  • Solutions
    • In Silico & Data Insights
      • Leadscope Model Applier
      • Knowledgescan
      • Advance
      • Predict
      • Centrus
    • Study Management
      • Climb
      • Pristima
      • Logbook
      • Provantis
      • Biorails
      • NOTOCORD-hem
      • Morphit
      • Comet Assay IV
      • Cyto Study Manager
      • Compliance Builder
      • Quality System Management (eQCM)
    • Regulatory Submission
      • SEND Advantage Services
      • Submit
    • Lab Execution
      • Matrix Gemini LIMS
    • Clinical Trial Analytics and Transparency
      • Accel
      • Aspire
      • Blur
      • Clinical Trial Transparency (CTT) Services
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