OK Capsule, a company that formulates, sells, and delivers personalized dietary supplements, has received certification of compliance with current Good Manufacturing Practices (cGMP). The certification ensures that OK Capsule has been inspected by an independent third-party auditor and provides a layer of assurance that products are of high quality and meet all current regulatory standards.

The GMP regulations define the quality and operations requirements for a product’s safety through four categories, including integrity, strength, purity, and quality. While the company said it has adhered to GMP regulations, mandated by the FDA, it has taken the extra step to become GMP certified by a third party.

“We are thrilled to be the first with the cGMP certification under our belt,” said Dr. Andrew Brandeis, CEO and founder of OK Capsule. “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.”

OK Capsule provides the technology, products, fulfillment, and strategic support to make it safe, simple, and sustainable for businesses to launch and scale the delivery of tailored supplement packets to customers. Dedicated to “redefining the industry” by enabling any brand, at any scale, to deliver personalized, high-quality supplements directly to consumers, the company said it has experienced “incredible growth” this year, including an array of new clients and raising $9.5 million in funding.

OK Capsule operates according to cGMPs under 21 CFR part 111 and part 117, with an FDA-compliant fulfillment facility in Reno, NV. By working within the cGMP regulations, the company will undergo audits on a regular schedule, in addition to periodic FDA inspections to guarantee that high-quality standards are being met with every sustainable package that is manufactured.