Third-Party COA Testing for Every Batch

Third Party Certificates of Analysis: Every Batch Tested Since 2007

RevGenetics Certificate of Analysis, every batch tested by ISO 17025 labs

We test EVERY batch. Not one batch for a marketing seal. RevGenetics pioneered public third-party Certificates of Analysis in 2007. Our CEO, family, and friends take these products, so we test every batch with ISO 17025 accredited laboratories.

Made in the USA, same certificates worldwide. Products sold on RevGenetics EU are manufactured in the same cGMP certified, FDA registered US facilities and carry the same batch certificates published below.

100%
Batches Tested
ISO
17025 Labs
2007
Pioneer
19+
Years
Anthony Loera, Founder and CEO of RevGenetics

Anthony Loera, Founder & CEO of RevGenetics

"My family, friends, and I take RevGenetics products every day. That's why we test every single batch with independent labs and publish the results publicly. We pioneered this transparency in 2007 because we believe you deserve the same quality assurance we demand for ourselves and our loved ones."

About Anthony: Founded RevGenetics in 2007 | 19+ years in longevity supplement formulation | Pioneer in third-party testing transparency | Learn more

The Problem with "Pay-to-Play" Single-Batch Testing

How the Supplement Industry Fakes Transparency

Many supplement companies pay a large one-off fee to services like ConsumerLab to test ONE batch of ONE product. If it passes, they get a seal they can use for marketing. But here is what they do not tell you:

  • One test is not every batch: that single test says nothing about the next 50 batches they produce
  • Failed tests stay hidden: if a company fails testing, results are "proprietary" and never published
  • Retesting is optional: products may only be retested every 12 months, if at all, to keep the seal
  • Marketing, not protection: the seal exists for marketing purposes, not ongoing quality assurance

The result: a company can pay for one successful test and then cut corners on every subsequent batch while proudly displaying their "certified" seal.

Industry "Standard" Testing

  • Pay a large fee to test ONE batch
  • Get marketing seal if it passes
  • Future batches NOT guaranteed tested
  • Failed tests kept confidential
  • Retest once per year, maybe
  • No personal stake in quality

RevGenetics Standard

  • Test EVERY batch before release
  • Publish COAs publicly for verification
  • ISO 17025 accredited labs only
  • Failed batches rejected and destroyed
  • CEO and family take these products

Why Most Supplements Are Not Properly Tested

The Testing Shortcuts Regulators Allow

58% of Facilities Have Violations

FDA inspections found that 58% of dietary supplement facilities were cited with cGMP violations. 19% failed to set specifications for identity and purity. 16% failed to verify ingredient identity through proper testing.

What Regulations Allow

  • Statistical Sampling: manufacturers can test only a subset of batches, not every batch
  • Testing Exemptions: petitions are allowed for exemption from 100% identity testing requirements
  • Supplier Qualification Shortcut: ingredient identity does not need lab verification if the supplier is "qualified"
  • Limited Enforcement: inspectors reach only a fraction of 13,000+ registered facilities
  • No Pre-Market Approval: supplements do not require approval before sale
  • Skip-Lot Testing: companies can skip testing on certain batches based on statistical models

What RevGenetics Does Instead

  • 100% Batch Testing: every single batch is tested before release, no exceptions, no statistical sampling
  • ISO 17025 Labs Only: only internationally accredited laboratories conduct our testing
  • Public COAs: results published for customer verification, not hidden behind paywalls
  • Full Panel Testing: identity, purity, potency and heavy metals on every batch used in our supplements
  • Personal Stake: our CEO, family and friends take these same products daily
  • Pioneer Since 2007: first supplement company to provide public COAs

Testing Standards Comparison

Why RevGenetics Testing is Different
Testing Practice RevGenetics ConsumerLab Seal Regulatory Minimum
Batch Testing 100% of batches 1 batch for seal Sampling allowed
Cost Model Internal commitment Large fee per product N/A
Future Batches All tested Not guaranteed Not required
Failed Test Results Batch rejected and destroyed Kept confidential Not disclosed
Public COA Access Yes, downloadable Seal only, no COA Not required
Lab Accreditation ISO 17025 required Labs not disclosed Not specified
Heavy Metal Testing Every batch, ICP-MS Single batch only Not explicitly required
Retest Frequency Every batch Every 12 months, if at all No requirement
Personal Stake CEO and family take products Marketing service N/A
Pioneer Status Since 2007 Since 1999 N/A

Why We Test Every Batch, Not Just for Marketing

"We Take What We Sell"

RevGenetics was founded in 2007 with a simple principle: we would never sell a product we would not give to our own family. Our CEO Anthony Loera, his family and his friends take RevGenetics products daily. This is not a marketing claim, it is the reason we test every batch.

When you protect your own family with your products, cutting corners is not an option. That is why we pioneered public third-party COAs and continue to test every batch 19 years later.

RevGenetics Quality Verification Protocol

How We Test Every Batch, Step by Step

  1. Raw Material Verification: every incoming ingredient is quarantined and tested for identity before use in manufacturing.
  2. In-Process Testing: quality checks during manufacturing ensure specifications are maintained throughout production.
  3. Finished Product Testing: complete analysis including identity (HPLC/FTIR), potency quantification and purity verification.
  4. Heavy Metal Panel: ICP-MS testing for lead, mercury, cadmium and arsenic on every batch, with results typically 100-800x below USP limits.
  5. Microbial Testing: where applicable, testing for total plate count, yeast, mold and pathogens.
  6. COA Publication: upon passing all tests, the Certificate of Analysis is published on this page for customer verification.

Failed Batches: any batch that fails testing is rejected and destroyed. Period. We never "retest to pass", adjust results, or make exceptions. This is why we confidently say our CEO, family and friends take the same products we sell.

Advanced NMN 1000

Product: Advanced NMN 1000

Pharmaceutical-grade NMN tested for purity (HPLC), identity and heavy metals. Every batch verified.

Advanced NMN 1000, every batch tested
Batch Date Purity / Potency Result Certificate
Current Batch
Finished product, Lot 071026
2026-07 1000 mg/serving PASS Download PDF
Current Batch
Raw material, Batch 20260401
2026-06 100% by HPLC-UV PASS Download PDF
Previous 2025-09 99.6% PASS Download PDF
Previous 2025-01 99.2% PASS Download PDF

Raw material and finished product are tested separately. The NMN raw material for this production run (Batch 20260401) assayed at 100% NMN by HPLC-UV against a 99% estimated level, with heavy metals by ICP-MS at 0.096 ppm lead, 0.037 ppm arsenic, 0.014 ppm cadmium and 0.007 ppm mercury. Finished capsules also contain the flow agents required for encapsulation, so the finished-product COA for Lot 071026 verifies identity, potency against the 1000 mg per serving label claim, and microbial safety rather than restating a raw powder purity figure. Both certificates are linked above and were issued by MS Bioanalytical, LLC.

MetaQuercetin SuperZ

Product: MetaQuercetin SuperZ

Micelle and ionophore technology for enhanced quercetin absorption with zinc support. Every batch tested.

MetaQuercetin SuperZ, every batch tested
Batch Date Purity Result Certificate
Latest Batch 2025-11 Verified PASS Download PDF

Senolytics 500 (Fisetin 500mg)

Product: Senolytics 500

High-purity Fisetin (98%+). Tested for identity and purity via HPLC. Every batch verified.

Senolytics 500 Fisetin, every batch tested
Batch Date Purity Result Certificate
Latest Batch 2025-07 98.7%+ PASS Download PDF

EGCG 800 (No Caffeine)

Product: RevGenetics EGCG 800

98% pure EGCG extract, caffeine-free. Tested for catechin content and caffeine absence. Every batch verified.

EGCG 800, every batch tested
Batch Date Purity Result Certificate
Latest Batch 2025-09 98.7% PASS Download PDF

MetaCurcumin Maximum Strength

Product: MetaCurcumin Maximum Strength

Liquid micelle curcumin capsules. Tested for curcuminoid content. Every batch verified.

MetaCurcumin, every batch tested
Batch Date Purity Result Certificate
Latest Batch 2025-11 Verified PASS View COA

RevGenetics Spermidine

Product: RevGenetics Spermidine (Rapymine)

Verified spermidine content. Every batch tested.

Spermidine, every batch tested
Batch Date Content Result Certificate
Latest Batch 2025-12 Verified PASS Download PDF

Resveratrol Products

Products:

99%+ pure trans-resveratrol, tested for purity and Emodin-free status. Every batch verified.

Resveratrol, every batch tested
Batch Product Purity Result Certificate
Latest Nitro500 / M98 material 99%+ PASS Download PDF
Latest X500 (500mg) 99% PASS Download PDF

TetraCurcumin Nano

Product: TetraCurcumin Nano

Nano-formulated tetrahydrocurcumin. Every batch tested. Certificate for the current batch is available on request while the document is being prepared for publication.

TetraCurcumin Nano, every batch tested
Batch Date Purity Result Certificate
Latest Batch 2025-08 Verified PASS On request

Frequently Asked Questions About Certificates of Analysis

What is a Certificate of Analysis (COA)?

A Certificate of Analysis is an official document from an independent laboratory that verifies a product's identity, purity, potency and safety. It confirms that what is on the label matches what is in the bottle, and that the product is free from harmful contaminants like heavy metals, microbes and adulterants.

Are the EU products the same as the US products?

Yes. RevGenetics products sold in Europe are manufactured in the same cGMP certified, FDA registered facilities in the United States, from the same tested batches. The certificates published on this page are the certificates for those batches.

Why did RevGenetics pioneer public COAs in 2007?

RevGenetics' CEO, family and friends all take RevGenetics products. We became the first supplement company to publish Certificates of Analysis publicly because we wanted the same transparency for our customers that we demand for ourselves. We test every batch because we personally consume what we sell.

What is wrong with ConsumerLab and similar certification services?

Services like ConsumerLab charge companies a large fee to test a single batch of a single product. If it passes, the company gets a seal for marketing. This does not guarantee future batches are tested. If a product fails, the results are proprietary to the manufacturer and never published. RevGenetics tests every batch, not just one for marketing purposes.

What does ISO 17025 accreditation mean?

ISO 17025 is the international standard for testing and calibration laboratories. It ensures that labs have demonstrated technical competence, proper equipment calibration, validated methods and quality management systems. RevGenetics only uses ISO 17025 accredited laboratories for third-party testing.

What happens if a batch fails testing?

Failed batches are rejected and destroyed. Period. We never retest to pass, adjust results, or make exceptions. This is why we can confidently say our CEO, family and friends take the same products we sell to customers.