The company operates according to cGMPs under 21 CFR part 111 and part 117, with an FDA-compliant fulfillment facility in Reno, NV.
OK Capsule (Reno, NV), which formulates, sells, and delivers personalized supplements, has achieved GMP certification of current Good Manufacturing Practices (cGMP) compliance. GMP regulations are mandated by the U.S. Food and Drug Administration (FDA), therefore OK Capsule has been adhering to them, but the extra step of being GMP certified by a third party provides a layer of assurance that the products produced will be of the highest quality and meet current regulatory standards.
“We are thrilled to be the first with the cGMP certification under our belt,” said Andrew Brandeis, ND, CEO and founder of OK Capsule, in a press release. “At OK Capsule, we are committed to pushing the standards and providing a unique and personalized experience. The future of medicine is personalization, and we are continuously looking for opportunities to break new ground in developing and adapting our technology.”
The company operates according to cGMPs under 21 CFR part 111 and part 117, with an FDA-compliant fulfillment facility in Reno, NV.
Magnesium L-threonate, Magtein, earns novel food authorization in the European Union
December 19th 2024According to the announcement, the authorization is also exclusive to AIDP and its partner company and licensee, ThreoTech, meaning that they are the only parties that can market magnesium L-threonate in the EU for a period of five years.