Quality is engineered into every product. Recognized for outstanding quality in more than 75 countries worldwide. Our manufacturing facilities operate under strict FDA Good Manufacturing Practices (GMP). Kosher, Halal and organic-certified, we have been audited and approved by leading independent bodies as well as by governmental health authorities worldwide.

On the quality assurance side of the business, we have dozens of employees dedicated entirely to making sure every step of production is top of the line quality and exceeds the expectations of our customers.

The Quality Assurance Department has broad responsibilities and authority in the following areas:

►     Quality Improvement — Quality improvement is based on the premise that all work activities can be planned, performed, measured, and improved. QA monitors our progress toward our corporate goal of building a culture in which improvement is continuous and an integral part of the organization.

►     Personnel GMP Training and Qualification — All employees who come into contact with our products must begin GMP training within the first month of employment. GMP training continues on a regular basis throughout the length of employment. Tests are given to monitor the effectiveness of training.

►     Internal Audits— QA inspectors monitor all phases of production to assess performance and adherence to GMP and to the SOPs of each department.

►     External Audits— QA oversees and supervises inspections and audits of our facilities by domestic and international regulatory bodies, as well as by customers and independent auditing firms.

►     Supplier Qualification — VITAQUEST maintains an audit program to verify our suppliers’ ability to provide consistent products that meet our strict quality requirements.

►     Document and Record Control — QA is responsible for maintaining all documents, records and Standard Operating Procedures, making sure that they are up to date.

►     Inspection and Acceptance Testing — QA has the authority to release and reject any component or finished product that does not meet specifications.

►     Non-Conformances — QA handles the identification, documentation, control, investigation and disposition of all non-conforming materials, components and final products.