Quality and Compliance
Quality systems designed for regulated healthcare environments
From US-based cultivation through laboratory processing and cGMP pharmaceutical grade manufacturing, NuNature Labs applies disciplined quality systems, documentation, and traceability across the production lifecycle. Our approach supports healthcare evaluation, institutional governance, and regulated market expectations while ensuring consistency and integrity across pharmaceutical-grade cannabinoid programs.
Our quality framework
Our quality approach begins at the source, with controlled agricultural inputs designed to support repeatability, documentation, and institutional review.
Controlled inputs and tracebility
Our quality approach begins at the source, with controlled agricultural inputs designed to support repeatability, documentation, and institutional review.
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US-grown industrial hemp cultivated with cGAP-aligned certification
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Organically aligned cultivation without pesticides, herbicides, or fungicides
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Seed to harvest traceability supporting the chain of custody documentation
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US-based sourcing and traceability are supported through NuNature Farms, our controlled cultivation platform.
Manufacturing integrity and readiness
Finished dosage forms are produced under pharmaceutical-grade quality systems designed to support institutional evaluation and regulated healthcare use.
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Pharmaceutical grade finished product manufacturing
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Documented batch release and specification controls
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Identity, purity, and contaminant review before release
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Packaging and storage condition verification
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NuNature Labs maintains a structured stability framework supporting shelf-life assessment and storage guidance
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Laboratory processing and quality oversight
Laboratory processing is conducted within controlled environments using documented procedures designed to support consistency, oversight, and secure handling.
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cGMP-aligned laboratory operations
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In-process controls supporting repeatability
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Batch documentation and verification procedures
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Finished formulations are developed to meet applicable federal requirements, with compliance verified prior to release.
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Documentation available for institutional review
NuNature Labs maintains comprehensive quality documentation suitable for healthcare and institutional evaluation, including:
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Certificates of Analysis and batch summaries
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Traceability documentation from inputs through finished product
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Quality management system overview (SOP categories)
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Storage, stability, and shelf-life framework
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Compliance-first communication
NuNature Labs maintains compliance-forward communication. All materials are written for healthcare partners, regulatory reviewers, and institutional oversight teams—not consumers. We do not use recreational imagery, retail wellness claims, or consumer CBD positioning.
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Our messaging emphasizes documentation, standardization, and clinical alignment consistent with regulated healthcare environments.
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Regulatory status and availability vary by market. Information is provided for institutional evaluation only and does not imply U.S. authorization.