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At Maxmedchem, we’re more than a supplement supplier—we’re your partner in achieving better health. With a steadfast dedication to quality ingredients, rigorous testing protocols, and transparent practices, we strive to exceed your expectations. Our ingredients warehouses are located throughout Europe and North America.
How Does Quality Affect Bioavailability?
We use the word bioavailability a lot, and it essentially refers to the body ability to digest, assimilate and use nutrients. How the body breaks down vitamins, amino acids and minerals can depend on many factors, including, you guessed it—the quality of a supplement. Supplements sourced from high-quality and reliable sources are more likely to contain pure and potent ingredients that can provide maximum benefits. In contrast, supplements sourced from questionable sources may contain contaminants or impurities that can affect bioavailability negatively.
Some amino acid ingredients, such as spermidine trihydrochloride, urolithin A, ergothioneine, in these cases, we produce high levels of molecular formulas such as biosynthetics to help improve the body antioxidant bioavailability.
Where are Maxmedchem Ingredients Manufactured?
Our in-house certified manufacturing Ontario, CA 91761, USA. We oversee every step of manufacturing to ensure the highest quality products. We weigh, mix, measure, encapsulate, bottle and ship each individual formula at our in-house lab.
What are the Different Types of Testing?
To ensure the highest quality, we ensure rigorous testing of all ingredients leaving our facility as well as finished formulations. We perform both in-house and third-party testing, including microbiological testing, physical testing, analytical concentration testing (e.g. ICP-MS, HPLC), and identity testing (e.g. FT-IR, TLC).
Microbiological Testing
Your first line of defence against disease-causing bacteria and toxins. Helps to detect microorganisms such as specific bacteria, pathogens, yeast, and mold.
Physical Testing
Determining if product characteristics are up to standard (ex. density, solubility, dosage weights).
Analytical Concentration Testing
Analytical concentration testing is used to verify the potency (raw ingredient) or dosages (finished products) of specific compounds. Techniques such as ICP-MS (inductively coupled plasma mass spectrometry) or HPLC (high-performance liquid chromatography) are commonly used. This allows us to quantify the concentration of active ingredients in our raw and finished products. These techniques also enable us to screen for the presence of unwanted components like residual solvents or heavy metals.
Identity Testing
All compounds we receive must pass identification testing before they can be used in manufacturing. Techniques such as FT-IR (fourier transform infrared) spectroscopy or TLC (thin layer chromatography) are typically used for this purpose.
How Do Choose Our Supplier and Source Our Ingredients?
Our primary objective is to deliver a formula that is unique to you, with absolutely nothing else added. Since we do not mass produce formulas, our production process is very unique and we require different, and often complex levels of manufacturing and quality standards, all of which we’ve outlined here. If you have any further questions about the quality of our products, our production facility, or our manufacturing process, Get in touch CONTACT US.
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