Reduce Preclinical Study Time
from Hours to Minutes

Leading drug discovery & development organization reduces preclinical
research study costs by more than 15% with Provantis®

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Submit™ with confidence.

Instem’s submit™-SEND tools and services are the most widely adopted in the industry, operating at over 45 sites across 15 countries

Prepare. Plan. Submit.

The leading eSource,
Proactive EDC System for
early phase clinical trials

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Reduce the traditional costs and time
associated with Target Safety Assessment
development by up to 50%

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Global Strength. Powerful Solutions. We reduce R&D timelines by helping clients efficiently access, capture, manage and enrich data.


Latest News

Instem To Deliver SEND Education Course and Showcase Leading Software Solutions at Safety Pharmacology Society Conference, Berlin

Instem Exhibiting and Presenting at Annual Safety Pharmacology Meeting

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Instem Introduces New SENDTrial™ Software for Trial Design Domain Creation

SENDTrial Software Solution Reduces Trial Design Domain Creation Time for Clients by Up to 80%

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ChemOn Selects Instem to Help Automate Preclinical Processes and Meet Growing Demand for SEND

South Korean Contract Research Organization to Deploy Provantis® for Preclinical Data Management and Submit™ Software for SEND Management

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Virtual Demonstrations

To help you evaluate systems, we believe that an initial, no-pressure demonstration carried out over the Internet is the way to go.

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