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Where are Codeage supplements manufactured and what are their quality standards?

3 min read

According to Codeage, all supplements sold within the United States are manufactured in US-based facilities. This domestic production is a key component of the brand's quality assurance, but it tells only part of the story concerning where Codeage supplements are manufactured and their overall quality control.

Quick Summary

Codeage supplements are manufactured in the USA for the American market, using high-quality global ingredients. Production occurs in cGMP-certified and FDA-registered facilities, with all batches undergoing strict third-party testing.

Key Points

  • US-Based Manufacturing: For the US market, Codeage supplements are manufactured in the USA in cGMP-certified, FDA-registered facilities.

  • Global Ingredient Sourcing: Codeage sources high-quality, and sometimes unique, ingredients from reputable suppliers around the world to ensure optimal quality.

  • Rigorous Third-Party Testing: All products undergo strict third-party testing for purity, safety, and potency, and have included heavy metals testing since June 2020.

  • cGMP Compliance: Production facilities adhere to Current Good Manufacturing Practices (cGMP), which are regulations set and enforced by the FDA to ensure quality standards.

  • Certificate of Analysis: Codeage obtains a Certificate of Analysis (COA) for every batch produced, offering transparency about product quality and test results.

  • Allergen Control: Facilities have strict allergen control protocols, and many products are free from common allergens like dairy, soy, and gluten.

In This Article

American-Made with a Global Approach

For customers within the United States, Codeage supplements are proudly manufactured domestically in the USA. This allows for closer oversight of the manufacturing process and adherence to national regulatory standards. While the manufacturing is local, the sourcing of the ingredients is global. Codeage emphasizes its dedication to procuring the finest, most potent ingredients from trusted suppliers worldwide. This combination of global sourcing and local manufacturing enables the company to access high-quality raw materials while maintaining control over the final production process in US-based facilities.

The Importance of Certified Facilities

Codeage places a high priority on partnering with manufacturing facilities that adhere to strict industry standards. All of their supplements are produced in facilities that are cGMP (current Good Manufacturing Practices) certified and registered with the FDA.

What does this mean for consumers? It means the facilities meet a high standard of cleanliness, processing, and record-keeping, ensuring products are consistently produced and controlled according to quality standards. Specifically, cGMP regulations enforced by the FDA govern every aspect of the manufacturing process, from raw material testing to final product labeling. For example, the Codeage beef organ supplements are made from grass-fed Argentinian cattle, which are processed via freeze-drying in these certified US facilities to preserve nutritional value.

A Comprehensive Quality Control System

Beyond domestic manufacturing and facility certifications, Codeage has a multi-layered approach to quality control. This system is designed to ensure that each supplement meets rigorous standards for safety, purity, and potency before it reaches the consumer. The key elements of their quality assurance process include:

  • Ingredient Vetting: Sourcing involves a stringent selection process for all global ingredients, focusing on quality, purity, and potency from reputable suppliers.
  • Certificate of Analysis (COA): Codeage obtains a COA for every batch of its products. This document confirms the quality, purity, and potency through detailed test results.
  • Third-Party Testing: All production batches undergo third-party testing by independent laboratories. This is a critical step for verifying the product's safety, purity, and potency. Since June 2020, this has also included testing for heavy metals.

This meticulous process ensures that what is stated on the product label is accurately reflected in the product itself.

Comparison of Manufacturing Standards

To better understand Codeage's commitment to quality, here is a comparison of their manufacturing practices versus generic, uncertified alternatives.

Feature Codeage Manufacturing Generic Uncertified Manufacturing
Location USA-based for US market Can be anywhere globally with varying oversight
Facility Certifications cGMP and FDA registered, sometimes NSF certified May lack any recognized certifications, or have lower standards
Ingredient Sourcing High-quality, globally sourced from vetted suppliers Potentially low-cost, low-quality, or contaminated ingredients
Product Testing Strict third-party testing for safety, purity, and potency Often relies on minimal or no independent testing
Transparency Provides Certificates of Analysis (COA) for batches upon request Little to no information available on testing or batch analysis
Ingredient Traceability Documented tracking of ingredients from vetted suppliers Limited or no traceability of ingredients back to their source

A Commitment to Purity and Transparency

Codeage’s manufacturing processes are a cornerstone of their brand's promise of purity and transparency. The use of global ingredients is viewed as an opportunity to source the best possible raw materials, and the strict manufacturing and testing protocols serve as a safeguard for consumer confidence. By choosing facilities that adhere to the highest standards, Codeage can also cater to specific dietary needs, offering many products that are non-GMO, dairy-free, and soy-free. Their dedication to providing Certificates of Analysis further demonstrates a commitment to open communication with their customers.

Conclusion

In conclusion, Codeage supplements sold in the U.S. are manufactured in the USA, in cGMP-certified and FDA-registered facilities. The process relies on globally sourced, high-quality ingredients that undergo rigorous, independent third-party testing for safety, purity, and potency, including heavy metals. This comprehensive approach to manufacturing and quality control is designed to ensure that the supplements consistently meet high standards, providing a transparent and trustworthy product for consumers. For more detailed information, consumers can visit the Codeage official website.

Official Codeage Website

Frequently Asked Questions

Yes, all Codeage supplements sold in the United States are manufactured in facilities located within the USA.

Yes, Codeage uses high-quality ingredients sourced from various locations around the world, which are then processed and manufactured in US facilities for the American market.

Yes, Codeage products are manufactured in facilities that are cGMP (current Good Manufacturing Practices) certified and registered with the FDA. Some facilities also hold NSF certification.

Yes, every batch of Codeage products undergoes strict third-party testing by independent laboratories to verify its safety, purity, and potency before being released to the market.

Yes, Codeage has been third-party testing all productions and lots for heavy metals since June 2020.

Codeage obtains a Certificate of Analysis (COA) for each batch of its products, and this information is available upon request.

Yes, their cGMP-certified facilities follow strict protocols for cleanliness and allergen control to prevent cross-contamination during manufacturing.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.