Our Process
In addition, our formulations are made according to FDA current Good Manufacturing Practices (GMP) using sanitary and well-controlled quality standards. Assurance of safe, sanitary, well-controlled, and well-documented manufacturing and monitoring processes indicates that the pharmacy is quality-conscious, and that all formulations will be manufactured with consistent quality from batch to batch. This formal system of controls also helps to prevent instances of contamination, mix-ups, deviations, failures, and errors.
Furthermore, every ingredient in our high-quality formulations is sourced from FDA-approved vendors and are independently verified by a third-party independent lab for quality assurance. We test each batch to detect dosing, potency, purity, stability, and sterility. This is a key quality measure that separates our supplements and prescription medications and most importantly the ingredients are verified for safety. With this level of testing, you can be sure that what’s on the label is what’s in the capsules.
Pharmacy Accreditation:
Certified as a “Center of Excellence” by the DynaLabs Continuous Improvement (CQI) Partnership Program, which is an Independent, third-party quality testing to ensure potency, purity, and stability. Our partnered pharmacy has demonstrated highly accurate and precise compounding, resulting in higher standards for patient safety.
Accredited by the Pharmacy Compounding Accreditation Board (PCAB). A voluntary certification denoting the highest standards of quality assurance, quality control and quality improvement. One of only approximately 150 PCAB accredited compounding pharmacies out of 56,000 pharmacies in the country.
Please be aware that not all compounding pharmacies are created equal. The sourcing of raw materials from safe vendors, formulation of these ingredients, manufacturing process, and testing are not all universal.
