Quality Assurance and Quality Control
Dee Cee Laboratories is committed to manufacturing the highest quality vitamin, supplement and nutritional products in the Dietary Supplement Industry. Dee Cee is confident that by producing high quality products, customer confidence will assure the mutual success.
Quality Assurance at Dee Cee includes writing and/or approving production procedures, writing specifications for raw materials and products, sampling and identifying all incoming materials, testing work-in-process (WIP), confirming identity, purity and potency of finished product, assuring package integrity reviewing production records for completeness and accuracy, and filing manufacturing documentation and retention samples for future evaluation.
Our experienced in house Food Scientist supervises all testing on vitamins, minerals, and supplements including:
- Physical Evaluations
- Ingredient Identity
- Stability Testing
- Hardness Testing (tablets)
- Friability (tablets)
All ingredients are in strict conformity to label, use, and packaging regulations in order to ensure product integrity.
Quality Assurance inspectors review in-process materials and documentation to assure compliance with product specifications and FDA regulations.
Work-in-Process (WIP) and finished products are evaluated by Quality Assurance to determine efficacy and compliance. Batches not meeting specifications are rejected to ensure quality throughout the process.
As each batch is completed, the Master Batch Record (MBR), finished goods, and laboratory tests are thoroughly reviewed and verified for accuracy by Quality Assurance before the product is given a final stamp of approval and released.
All processes are governed by Current Good Manufacturing Practices (CGMPs). Raw material ingredients and supplies are quarantined upon receipt. After appropriate sampling and testing, a quality release is granted to materials conforming to specifications. Nonconforming materials in any stage of production are rejected. Only released materials and products can advance to the next stage of production.
Our manufacturing and packaging facility is registered with and inspected by the FDA. Dee Cee's FDA Facility Registration # is 1023013. Our products are manufactured under Current Good Manufacturing Practices (CGMPs). This, along with the dedication of our employees is why you can depend on the quality, potency, and purity of our products.