We are honored to announce that Alise Pharma has been named one of the Top 10 Supplement Brands by the Clean Label Project, a national nonprofit organization dedicated to health and transparency in consumer products. This recognition reflects years of deliberate investment in ingredient sourcing, manufacturing standards, and radical transparency across every product in our lineup.

In an industry where label claims are not always backed by rigorous verification, this award signals to our customers that Alise Pharma holds itself to a higher standard. Here is a closer look at what the Clean Label Project is, what their evaluation process entails, and what this distinction means for you.

What Is the Clean Label Project?

The Clean Label Project is an independent, nonprofit organization that tests consumer products for both label accuracy and contaminant safety. Unlike many certification programs that rely on self-reported data, the Clean Label Project purchases products directly from retail shelves and submits them to accredited third-party laboratories for analysis.

Their testing protocol screens for over 400 environmental and industrial contaminants, including heavy metals such as lead, mercury, cadmium, and arsenic, as well as pesticide residues, plasticizers, and other substances that rarely appear on product labels. The project also verifies that what is listed on the label matches what is actually in the bottle -- checking for both the presence and the dose of every active ingredient.

To date, the Clean Label Project has tested over 80,000 products across dozens of consumer categories, making it one of the most comprehensive independent testing initiatives in the supplement and food industries.

What the Award Recognizes

The Top 10 designation is not given lightly. Brands are evaluated across multiple dimensions, including ingredient purity, label accuracy, contaminant levels, and overall manufacturing consistency. Of the hundreds of supplement brands evaluated in the 2025 cycle, only ten earned this distinction.

Alise Pharma scored in the top percentile for label accuracy, meaning the active ingredient quantities listed on our labels consistently matched independent laboratory measurements within a tight margin of variance. Our products also demonstrated contaminant levels well below established safety thresholds set by organizations such as the FDA and the World Health Organization.

Importantly, the evaluation also considers a brand's track record over time. This is not a one-time snapshot but a cumulative assessment of consistency and reliability across multiple product lines and manufacturing batches.

Our Commitment to Transparency

From the day Alise Pharma was founded, transparency has been a core operating principle rather than a marketing tagline. Every product page on our website lists the full ingredient panel with exact dosages -- no proprietary blends, no hidden fillers, no ambiguous "complexes" that obscure what you are actually consuming.

We publish Certificates of Analysis (COAs) for every production batch, making them accessible directly from each product's page. These documents detail the results of identity testing, potency verification, heavy metal screening, and microbial analysis. Customers can cross-reference the batch number on their bottle with the corresponding COA to verify exactly what is in their product.

We also maintain a public list of every raw material supplier we work with, along with the certifications and quality accreditations they hold. This level of supply chain visibility is uncommon in the supplement industry, and we believe it should be the norm.

Third-Party Testing Practices

Alise Pharma partners with multiple ISO 17025 accredited laboratories to conduct independent testing at every stage of production. Raw materials are tested upon receipt before they enter our manufacturing facility. In-process testing is performed during blending and encapsulation. And finished products undergo a final round of third-party analysis before they are released for sale.

This three-stage testing protocol ensures that contamination or potency issues are caught early and corrected before a product reaches the customer. In the rare event that a batch does not meet our specifications, it is rejected and disposed of in accordance with FDA guidelines -- it never ships.

Earlier this year, we expanded our testing program by partnering with an additional accredited laboratory, effectively doubling our testing throughput. This allows us to perform batch-level COAs on every SKU we produce, rather than relying on periodic sampling.

What This Means for Our Customers

For customers, this recognition provides an independent, third-party validation that the products they are purchasing meet the highest standards of quality and safety in the industry. It means you can trust that the label on your Alise Pharma supplement accurately reflects what is inside the bottle.

It also reinforces our commitment to continuous improvement. The Clean Label Project's evaluation framework is updated annually to reflect emerging research on contaminants and new analytical methodologies. By maintaining our standing in this program, we ensure that our quality systems evolve alongside the science.

We view this award not as a finish line but as a milestone on a longer journey. Our goal has always been to set the standard for quality in the supplement industry, and the Clean Label Project's recognition confirms that we are on the right path. We are deeply grateful to our customers, our manufacturing partners, and our quality team for making this possible.