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Physical property testing ensures dosage forms like tablets, capsules, and sprays perform as intended. These tests confirm quality, consistency, and safety in compliance with Canadian standards.
We adhere to established industry standards and reference methods, including ISO, Health Canada Standards, and other relevant guidelines. This ensures the reliability and comparability of our testing results. Our methods are continuously updated to reflect the latest advancements in materials testing.
To confirm that dosage forms like tablets, capsules, and sprays perform consistently, meeting safety and regulatory standards.
Disintegration measures how fast a dosage form breaks apart, while dissolution measures how much and how quickly the active ingredient is released into solution.
Yes. Health Canada requires NHPs to meet pharmacopeia standards for consistency and performance, not just pharmaceuticals.
They demonstrate bioavailability, bioequivalence, and batch consistency, which are essential for regulatory approval and patient safety.
Yes, especially for fortified or functional foods, powders, and chewables, to ensure nutrients are released properly.
Products like lozenges or effervescent tablets rely on disintegration and dissolution to verify consistent delivery of active ingredients.
Health Canada adopts USP standards alongside the Natural Health Products Regulations and Food and Drugs Act.
Regular calibration is required under GMP to ensure accuracy, with documentation available for audits and inspections.
A method (coming soon) for sprays, pumps, and inhalers that confirms each actuation delivers a consistent dose throughout the container’s life.
