cGMP Manufacturing and Packaging Facilities

Alistrol wants you to feel confident that our product is safe and will meet your expectations. Be assured that Alistrol is produced in accordance with the Dietary Supplement Health and Education Act (DSHEA) of 1994. All employees who come into contact with our products have been trained in cGMPs (current Good Manufacturing Practices) as defined by the Food and Drug Administration.

There are five key areas in our quality assurance system:

• Quality Administration:  Monitors process control and continuous process improvement. This area includes employee training, records retention, quality, and safety.

• Incoming Material Control:  Manages all incoming materials including pre-inspection quarantine, inspection and acceptance plans, and a non-conforming material plan.

• Supplier Qualification: Our suppliers are evaluated and selected for their adherence to the same high standards and cGMPs that Alistrol abides by. No products are accepted into our facility without a Certificate of Analysis, Material Data Safety Sheet (if applicable), and a Standard Operating Procedure Certificate.

• Outgoing Product Control: Includes final product inspection, shipping audits, and final batch records.

• Document Control: This includes policies, master plans, instructions, records, change control, and product numbering and revisions.