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March 23-26, 2026
New York City
Our Methodology
We run natural health programs with a disciplined path from development to release-ready supply.
Develop and Secure the formulation
We optimize the formulation and process manufacturing to support manufacturing reproducibility.
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Scale-up and transfer the process
We execute scale-up runs and finalize batch documentation to enable reliable routine production.
Produce under GMP standards
We perform manufacturing and packaging under GMP conditions through finished packaged lots.
Release and lifecycle support
We deliver release-support testing, review documentation, and manage updates through controlled change.
Our Capabilities
We support NHPs from development to release documentation, aligned with Health Canada NPN and DIN‑HM pathways.
NPN
For NPN products, we deliver development and controlled CDMO execution with documentation and quality controls that support your product licence file and routine supply.
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Formulation and process work designed for transfer and commercial production.
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GMP-aligned batch records and traceability, structured to fit site licensing expectations for manufacturers, packagers, and labellers.
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Homeopathy
For homeopathic medicines, we support DIN‑HM programs with packaging execution and traceable documentation aligned with Natural Health Products Regulations.
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Controlled handling and documented workflows that carry product identity through finished packaged lots.
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Packaging and labeling execution planned for market needs, with the DIN-HM identification approach reflected in the documentation.
Our Services
Services that move NHP and homeopathic products from development to release-ready supply.
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Product Development
Formulation and process work designed to transfer cleanly into scale-up and routine batches.
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Analytical Services
Testing and documentation that support clear specifications, batch decisions, and product files.
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Manufacturing & Packaging
Controlled execution and packaging operations that protect product integrity through finished goods.