02.05.10
Robinson Pharma Inc., (RPI) Santa Ana, Ca, has completed a surveillance audit for GMP compliant manufacture of dietary supplements to the standards outlined in 21CFR Part 111. The audit was performed by STR, a leading global third party testing and auditing firm focused on quality systems and analysis. The STR quality systems audit assesses the ability of a company’s manufacturing process to effectively and consistently produce correctly labeled, pure, and safe product.
STR analyzed the RPI Standard Operation Procedures (SOPs), staff qualifications, staff training program, and facility adequacy and cleanliness. All aspects of the manufacturing process were reviewed including receipt and authentication of ingredients, the production process, post production product analysis, product handling, packaging, storage and record keeping. RPI, which holds a drug manufacturing license issued by the state of California, was shown to comply with the standards mandated by the STR RQP. The RQP standards were originally created to assure safely, purity, and label claim compliance for dietary supplements marketed in a leading national retail chain.
