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Made Group quality standart.

Quality Control.

We are deeply committed to crafting the highest quality product possible. Leveraging state-of-the-art technology and quality control measures, we manufacture flawless capsules, ensuring the absence of imperfect capsules, loose powder, irregular ingredients, or any subpar outcomes.

Throughout each stage of production, records are maintained, documenting the origin of each ingredient used in every batch, enabling accountability.

Our material purchaser possesses expert knowledge of the raw ingredients that align with our company's quality standards. Regular checks against third-party laboratories ensure these ingredients consistently meet our exacting expectations.

Heavy Metal Testing

Microbiological Testing

To ensure the raw materials meet our standards, we carry out rigorous heavy metal testing, detecting the presence of lead, mercury, cadmium, and arsenic. Upon passing these tests, the materials are inventoried and stored in designated locations according to their specific storage requirements.

Once confirming the uniformity and even distribution of the blend, we verify the nutrient potency of each tablet by ensuring they have the correct weight, also known as content uniformity.

Throughout production, as tablets are punched and capsules filled, their weight is consistently measured to maintain uniformity. Alongside routine tests for weight uniformity, we also record thicknesses and densities.

Any deviations from expected standards lead to rejection; only products meeting our specifications are accepted.

Uniformity of Mix

Content Uniformity

Dissolution Testing

In the blending stage, all ingredients for a particular dietary supplement undergo thorough mixing to achieve uniform distribution across the batch. This crucial step guarantees that every capsule, tablet, or powder contains precisely measured nutrients consistent throughout the entire batch.

Following blending, a sample of the mixture is extracted and sent to the lab for rigorous quality assurance testing. Approval for shipment and use is granted only when the sample meets our stringent standards.

Stability Testing.

Stability testing aids in pinpointing the nutrients most susceptible to degradation or reduced effectiveness and determines the extent of potency adjustment required to offset degradation effects over time. This process utilizes two distinct methods.

Accelerated Stability

Ambient Stability

In accelerated stability testing, a dietary supplement in its original packaging is enclosed within an environmental chamber, regulating temperature and humidity to simulate accelerated aging conditions. For instance, if the product undergoes one month in the accelerated machine, it might equate to approximately six months of natural aging. After removal from the chamber, the product undergoes evaluation to determine any decline in potency and assess any other potential impacts.

Ambient stability assessment involves storing packaged product samples in a room with controlled temperature and humidity, allowing us to observe the effects of time on the products without resorting to accelerated testing. Periodic potency tests are conducted during this process, enabling comparisons between laboratory-generated data and real-world performance data.

Finished Products.

Once the production batch of finished tablets is complete, a series of tests similar to those conducted on the raw materials is repeated. These tests encompass raw material identity and potency, microbiological analysis, and heavy metal screening.

Following the completion of a batch, thorough equipment cleaning takes place to prepare for the subsequent product. The duration of the cleaning process varies depending on the machinery used, ranging from two to twelve hours.

Comprehensive machine cleaning logs are documented and retained for future reference.