Learn how Instem’s Samarind RMS
software solution can “Unlock the
Potential of Your Medical
Device Licenses”

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Learn how an Instem client has dramatically
reduced Target Safety Assessment production
timescales with our KnowledgeScan™ service.

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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 80 sites across 15 countries

Prepare. Plan. Submit.

Cyto Study Manager is revolutionizing
GeneTox Study Workflows

Helping clients to reduce costs, increase efficiencies
and improve regulatory compliance
.

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Setting the Standard in Target Safety Assessment

Combining computer-aided data acquisition & manipulation,
automated workflows, and scientific expertise, to deliver
detailed insight in biological target profiling.

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We enable our clients to bring their life enhancing products to market faster


Latest News

Jiangsu Provincial Institute of Materia Medica Selects Provantis Preclinical SaaS Solution

Provantis to Increase Efficiencies and Further Improve Study Data Quality at Nanjing Research Facility

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FDA SEND 3.1 Mandate Goes Into Effect

Scope of SEND Widens to Include Support for Cardiovascular and Respiratory Studies

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Instem to Showcase Deep RIM Capabilities at DIA’s Upcoming RSIDM Exhibition

Instem to Present Single-Place-of-Truth™ Approach for Regulatory Affairs Professionals

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Virtual Demonstrations

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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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We are excited that you have decided to take the next step with Instem. To provide you with an accurate quotation, we ask that you fill out our form.