A wide range of PuraCap products are manufactured by our affiliated manufacturing partner, Humanwell Puracap Pharmaceuticals (Wuhan) Co., Ltd, a US FDA cGMP compliant facility that complies with international regulatory standards. Our goal is to put quality first, by building quality through design and a commitment to the highest standards. We strive to exceed USFDA, cGMP standards to assure our customers the quality product they expect.
The experienced manufacturing team, led by a well-recognized technical manufacturing authority in the soft gelatin pharmaceutical capsule industry, is committed to growing our business responsibly – utilizing proven and innovative processes and procedures to produce quality products without compromise. The manufacturing team is backed by a U.S. executive team with decades of experience in FDA (Federal Drug Administration) regulated prescription drug cGMP quality system management and process validation.
The manufacturing team strives to provide cost-efficiency through manufacture at state-of-the art facilities built to USFDA specifications. Our model for success is to make use of labor as well as manufacturing efficiencies while meeting the highest quality standards. This model sets us apart from the competition. Our customers can be confident in our products—-highest quality at a competitive price. Our assurance is high quality, reliable products using the latest state of the art equipment including:
- Gelatin mixing/melting stations
- Pharmaceutical mixing/heating/cooling stations, in independent suites
- 6×10″ encapsulation machines in independent suites
- Enhanced capsule drying technologies
- In process test instrumentation
- Independent capsule inspection suites
- Independent capsule printing suites
- Independent capsule packaging suites
- Full bottling and blistering line capabilities in an independent suites
Located in the Wuhan National Bioindustry Base (Biolake) at East Lake National Innovation Demonstration Zone, learn more HERE.