Our Testing Process

Laboratory Transparency

How Golden Shilajit Is Tested

Golden Shilajit uses independent laboratory testing to document specific characteristics of finished product batches. Independent laboratory testing is documented on a batch-specific basis. Published testing has included Eurofins Scientific and Anresco Laboratories for heavy metals, Eurofins Scientific and TTI for fulvic acid, and Bureau Veritas for microbiological testing. Laboratory coverage and analytical scope can differ by batch. Laboratory results apply to the tested sample and batch, and should not be treated as permanent guarantees for every future batch.


Testing Starts With the Finished Batch

Manufacturing and laboratory testing are two separate stages. Purification produces the finished resin. Laboratory testing then measures selected characteristics of that finished batch.

Our water-based multi-stage purification process is documented separately. See: Our Manufacturing Philosophy. What this page covers is what happens after purification is complete — the independent laboratory analysis that documents what the finished batch actually contains.

Testing does not replace purification. Purification does not replace testing. They serve different purposes and are conducted independently of each other.


From Finished Batch to Lab Report

The steps below describe, at a high level, how a finished batch moves from production to independently documented laboratory result.

  1. A finished production batch is identified and assigned a batch reference number.
  2. A representative sample is prepared for independent laboratory testing.
  3. Samples are submitted to accredited independent laboratories according to the testing required.
  4. Laboratory results are received, reviewed, and associated with the tested batch reference.
  5. Batch-specific documentation is made available through the Lab Reports page.
These steps describe the general process at a high level. They do not represent a formally published standard operating procedure and should not be read as a complete technical specification of sampling methodology or chain-of-custody documentation.

Batch SLJT01LQ — Eurofins Scientific (Fulvic Acid & Heavy Metals)

Eurofins Scientific independently analysed the fulvic acid content and heavy metals of finished batch #SLJT01LQ. Eurofins is an ISO/IEC 17025-accredited laboratory. For a detailed explanation of how Eurofins conducts this analysis, see: how Eurofins tests Shilajit.

Batch-Specific Result — Batch #SLJT01LQ — Report 4999802-0 45.39 g/100g Fulvic acid content as reported by Eurofins Scientific for tested batch #SLJT01LQ. This result applies to this batch only and is not a guaranteed minimum or permanent specification.
Shilajit is a naturally formed geological material. Fulvic acid concentration varies between batches. Independent laboratory testing documents the result for each specific batch tested — it does not establish a fixed value that applies to all batches.

Full COA for batch #SLJT01LQ: Lab Reports page.


Batch SLJT01LQ — Bureau Veritas (Microbiological)

Microbiological testing for batch #SLJT01LQ was conducted independently by Bureau Veritas — Report No. 1086405.

Coliforms<10 cfu/g
Bacillus cereus<10 cfu/g
SalmonellaNot detected in 25g
E. coli<10 cfu/g
Aerobic colony count at 30°C<10 cfu/g

<10 cfu/g indicates count was below the detection threshold — not zero. Results are batch-specific.


Batch HI-SHL-0226 — Independent Laboratory Testing

Batch HI-SHL-0226 was independently tested by three laboratories. Results are batch-specific and documented in the corresponding reports published on the Lab Reports page.

Laboratory Scope Reference
Eurofins Scientific Fulvic acid & heavy metals (Pb, As, Cd, Hg) Report 5374116-0, Sample 16388887
Anresco Laboratories Heavy metals ICP-MS (Pb, As, Cd, Hg) Order 960349, Sample 1352051
TTI Fulvic acid testing Batch HI-SHL-0226
Batch HI-SHL-0226 was tested by multiple independent laboratories for cross-verification. Numerical results for each parameter are documented in the corresponding certificates published on the Lab Reports page.

What Each Laboratory Test Actually Tells You

Test Laboratory What It Documents
Fulvic Acid Eurofins Scientific, TTI Reported fulvic acid result for the tested sample, expressed as g/100g
Heavy Metals (Pb, As, Cd, Hg) Eurofins Scientific, Anresco Laboratories Measured heavy metal results for the tested sample
Microbiological Testing Bureau Veritas Reported microbiological results including coliforms, E. coli, Salmonella, Bacillus cereus, and aerobic colony count

What Laboratory Testing Does Not Prove

A laboratory report does not automatically prove:
  • Clinical effectiveness for any health condition
  • That every future batch will have identical results
  • Complete absence of every possible contaminant not included in the test scope
  • That one product is objectively “the best” Shilajit available
  • Product suitability for every individual, regardless of health status or medications

What a laboratory report does establish is a documented, third-party record of the specific parameters tested on the specific batch submitted.


Batch-Specific Transparency

A laboratory report is only meaningful when it can be tied to a specific batch. For guidance on reading a COA, see: how to read a Shilajit Certificate of Analysis.

Detail Why It Matters
Batch number Identifies which production run was tested. Results from one batch do not automatically apply to another.
Report date Confirms when testing was conducted.
Laboratory identity Confirms who conducted the analysis. Independent, accredited laboratories carry more evidential weight.
Analytes tested Specifies exactly what was measured. A COA only covers the parameters listed.
Numeric results The actual measured values, not just a pass/fail statement.

Documented batches: #SLJT01LQ and #HI-SHL-0226. Corresponding reports are available on the Lab Reports page. For the complete verification record covering both batches, see the Batch Verification & Laboratory Evidence hub.


Manufacturing vs Testing

Manufacturing

  • Water-based multi-stage purification
  • Multi-stage filtration
  • Controlled concentration
  • Natural sun drying

Laboratory Testing

  • Fulvic acid (Eurofins, TTI)
  • Heavy metals: Pb, As, Cd, Hg (Eurofins, Anresco)
  • Microbiological (Bureau Veritas — SLJT01LQ)

For the full purification process, see: Our Manufacturing Philosophy.


Lab Verified. Choose Your Size.

You’ve reviewed how Golden Shilajit is tested. Choose the format that best fits your order.

Golden Shilajit Resin 50g — $110Shop Resin 50g
Golden Shilajit Resin 100g — $180Shop Resin 100g
Golden Shilajit Drops 30ml — $80Shop Drops

View the Actual Reports

Batch-specific Certificates of Analysis from all laboratories are published openly — no sign-up required.


Frequently Asked Questions

Who tests Golden Shilajit?

Golden Shilajit is independently tested by Eurofins Scientific (fulvic acid and heavy metals), Anresco Laboratories (heavy metals ICP-MS), TTI (fulvic acid), and Bureau Veritas (microbiological testing). All are independent of Golden Shilajit and have no commercial interest in the outcome.

What was the fulvic acid result for batch #SLJT01LQ?

Eurofins Scientific reported 45.39 g/100g for tested batch #SLJT01LQ (Report 4999802-0). This result is specific to that batch and is not a guaranteed minimum or fixed specification for all batches.

Which laboratories tested batch HI-SHL-0226?

Batch HI-SHL-0226 was tested by Eurofins Scientific (Report 5374116-0, fulvic acid and heavy metals), Anresco Laboratories (Order 960349, heavy metals ICP-MS), and TTI (fulvic acid). Full reports are published on the Lab Reports page.

Does every batch have exactly 45.39% fulvic acid?

No. 45.39 g/100g is the documented result for batch #SLJT01LQ only. Shilajit is a naturally formed geological material and fulvic acid concentration can vary between batches. Each batch is tested independently.

How can I see the current Golden Shilajit lab report?

Current published laboratory documentation can be viewed on the Golden Shilajit Lab Reports page. No sign-up or request form is required.