Our clients trust our protocols for FDA pre-market product approvals, backed by over 50 years as an industry-leading research provider. Our expert team works with you to customize comprehensive cannabis data collection solutions that deliver reliable, actionable data.

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Achieve Regulatory
Body Approval

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Bring Your Product
To Market Faster

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Substantiate
Unique Claims

Supporting a Broad Range of Testing

Label Comprehension​

Actual Use Tests (AUT)​

Claims Substantiation​

Product Testing​

Behavioral Research​

Observational Studies​

User Experience​

Packaging Design​

Regulated Data Collection Expertise

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Extensive experience with
successful PMA submissions

Our expertise in recruiting subjects provides unparalleled access to your intended audience with secure data as mandated by the FDA.

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Rigorous project execution

Our team works closely with you to develop or follow clinical study protocols, manage interactions with the IRB, and deliver quality results nationwide efficiently to support your FDA reporting needs.

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Connect with Your Consumers

Our deeply profiled proprietary panel of opted-in consumers and patients powers our ability to connect you with your target audience for your important cannabis studies.

consumables

Consumable Users

medicinal

Medicinal Users

recreational

Recreational Users

Schlesinger NYC

Integrated Proprietary Data Collection Sites

Our world-class Schlesinger Group insights, testing, and simulation sites are located in key markets across the US and Europe. We coordinate all aspects of clinical research in each location with consistently high quality.

EXPLORE OUR LOCATIONS

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At Schlesinger Clinical Research, our expertise in participant recruiting and clinical project execution provides unparalleled access to your target audiences for data you can trust. Certified teams and 30 proprietary sites across key markets in the US, together with one Clinical Project leader, provides study consistency and quality to your timeline.

Have a project in mind?