Third Party Testing

Quality Documentation

Certificate of Analysis Library

Search available third-party testing documents by product name or category. Our library is continually updated as independent third-party testing is completed.

Document Transparency

A growing library of verified reports.

Search by product name to review the latest testing document currently published in our library.

  • Search by product name
  • Review report dates
  • Open available PDF reports
  • See pending-document status
COA Library Update

Our Certificate of Analysis library is continually expanding as additional products complete independent third-party testing. We believe in transparency and publish available laboratory reports as they are received rather than displaying only selected results. Because testing is ongoing, reports may be added, updated, or replaced over time to reflect the most current available testing documentation. Some blended products may be supported by testing documents for their individual components rather than a separate finished-blend report.

Search the Library

Currently available testing documents

Our current library is limited while additional products undergo third-party testing. New reports will be added as they become available.

Our COA library is currently being expanded.

Additional products are undergoing third-party testing. Finalized reports will be published here as they become available.

Understanding the Library

How to review a COA listing

Find your product

Search by product name to locate the latest Certificate of Analysis currently available in the library.

Review report details

Confirm the product identity, laboratory, report date, and reported testing scope shown in the PDF.

Check document status

Available means the report is linked. Pending means testing or document processing has not yet been completed.

Frequently Asked Questions

COA library questions

What is a Certificate of Analysis?

A Certificate of Analysis is a laboratory document reporting the testing performed on a submitted sample and the results issued by the laboratory.

Why are not all products listed?

Our COA library is continuously expanding. Some products are currently undergoing independent third-party testing, and finalized reports will be published once they become available.

Why is a report marked pending?

The sample may still be under testing, the final report may not yet be issued, or the document may still be awaiting publication.

Are blended products tested as a finished blend?

Testing practices may vary. In some cases, documentation may be available for the individual compounds used in a blend rather than the finished blended product itself.

Is a purity result below 99% acceptable?

A reported purity below 99% does not automatically indicate a quality issue. Manufacturers establish their own acceptance specifications based on the specific compound, manufacturing process, validated analytical methods, and internal quality standards. Because these specifications can vary, acceptable purity ranges are not necessarily identical across all manufacturers or products.

Depending on the manufacturer’s established specifications, purity values between 95% and 99% may still meet the applicable acceptance criteria.

At Mile High Peptides LLC, we believe transparency is an important part of quality. We do not try to hide or selectively publish only the highest results. We make available independent third-party Certificates of Analysis as they are received, including results that may vary between products or testing periods.

A Certificate of Analysis should be reviewed as a whole, including identity confirmation, analytical methodology, and any other testing reported by the laboratory—not purity alone.

Why do purity specifications differ between manufacturers?

Every manufacturer establishes its own acceptance specifications based on the specific compound, manufacturing process, validated analytical methods, and internal quality standards. As a result, acceptable purity specifications may differ between manufacturers and products.

For this reason, comparing products solely by a single purity percentage can be misleading. The complete Certificate of Analysis provides a more meaningful assessment than purity alone.

Will Certificates of Analysis change over time?

Yes. Testing is an ongoing process, and our COA library is a living resource. As additional products, production runs, or samples are independently tested, reports may be added, updated, or replaced to reflect the most current laboratory documentation available.

A report published today may differ from a report published later as new testing is completed.

Why aren’t all concentrations tested individually?

Not every concentration of a product is necessarily submitted for separate third-party testing. In some cases, multiple concentrations are prepared from the same active ingredient or source material that has already undergone quality testing.

Depending on the manufacturer and production process, testing may be performed on the active ingredient, representative production samples, or other quality-control samples rather than every individual concentration. Manufacturers establish their own testing protocols and acceptance specifications based on their production and quality-control procedures.

At Mile High Peptides LLC, we publish available third-party Certificates of Analysis as they are received. Because testing is ongoing, additional reports may be added or updated as new products, concentrations, or production runs are independently evaluated.

What should I do if a product is not listed?

If a product is not yet listed, it may still be undergoing independent third-party testing. Contact Mile High Peptides LLC support with the exact product name if you have questions about its current testing status.

Need Help Locating a Report?

Tell us which product you are looking for.

Include the exact product name so the Mile High Peptides LLC support team can help confirm whether a report is currently available or still undergoing testing.

Contact Support
Testing documents are provided for informational and quality-documentation purposes. Each report applies only to the sample identified in the applicable laboratory document and should be reviewed together with the testing methodology and reported results. Testing is ongoing, and reports may be added, updated, or replaced as new laboratory documentation becomes available.