Expert Medical Commission Iverylab

Purpose. Conducts scientific and technical evaluation of products for compliance with the requirements of safety, quality and evidence, and makes one of the decisions: include in the Iverylab catalog, include with conditions (improvements/additional data) or refuse (with reasons).

Evaluation stages.

1. Receipt and preliminary verification of documentation.

• Registration / notification documents (if required in the relevant jurisdiction).

• Right of official use from the manufacturer (for foreign brands — a letter or a power of attorney to the applicant).

• Reconciliation of composition and claims with documentation and specifications.

2. Expert evaluation by the iverylab commission.

• Analysis of composition, dosages, delivery forms, raw-material quality and excipients.

• Verification of materials on safety and efficacy.

3. Decision of the commission.

• Include in the iverylab catalog, include with conditions or refuse — with fixation of grounds (scientific, quality-related, documentary).

Criteria and scientific definitions.

1) High bioavailability of active substances.

Bioavailability is the fraction and the rate of entry of the active substance into the blood in an unchanged form. The Iverylab brand gives preference to forms and technologies that demonstrate better bioavailability of active substances when supporting data are available.

A separate pride of the Iverylab brand is the choice of complex production technologies to achieve the best bioavailability. These include: liposomal encapsulation, micellar technology of packaging active substances, thermozymal extraction, CO2 extraction, technologies of slow and stepwise release, and others.

2) Optimal dosages.

Taking into account the increased bioavailability of the selected components, it is possible to achieve a lower dosing per intake. At the same time, efficacy remains consistently high.

3) Mutually complementary components of the composition.

The components in the composition of Iverylab products are selected so as to complement each other, enhancing the effect from taking the dietary supplement.

4) High quality of raw materials.

Only high-quality, certified raw materials that have passed laboratory tests are used for our products. This provides a guarantee of safety and high bioavailability of finished products.

5) Excipients (auxiliary substances).

In the production of Iverylab products, compounds and substances dangerous for humans are not used. These include: titanium dioxide, acesulfame, aspartame, sodium lauryl sulfate, chlorine, propylene glycol, shellac, polyethylene glycol.

In quantities permitted by sanitary standards, the following may be used: lactose, sucrose, maltodextrin.

6) Production quality control.

Support of quality control in production is carried out by the ISO 22000:2018 compliance standard. This makes it possible to avoid admission to production of dangerous, toxic, harmful substances.