! For Research Use Only · Not for Human or Veterinary Use · Not Approved by the FDA or Health Canada for Any Therapeutic Purpose
3rd-party tested · 99.4% purity Free cold-chain shipping over $150 Subscribe & save 15%
EN / USDHelp

The Method.

Five independent tests. Full chromatograms published per lot. cGMP synthesis in Basel. This is what pharmaceutical-grade actually means — and why most vendors don't do it.

Five tests.
Every batch.

Most peptide vendors run a single HPLC pass and call it verified. Zenova runs five independent tests through an ISO 17025 accredited laboratory — and publishes the results, not a summary.

01 · Identity

Identification

High-resolution mass spectrometry confirms the exact molecular identity of each peptide. Sequence verified against the reference standard.

02 · Purity

Purity

Reversed-phase HPLC measures purity against total peak area. Zenova minimum threshold is 99% — above the 98% industry standard.

03 · Potency

Potency

UV absorbance verifies that each vial contains the stated quantity within ±2%. You get what the label says, to the milligram.

04 · Endotoxin

Endotoxin

Limulus Amebocyte Lysate (LAL) assay tests for bacterial endotoxin. Our limit is <0.05 EU/mg — far below the USP threshold for injectable preparations.

05 · Metals

Heavy Metals

ICP-MS screens for lead, arsenic, cadmium, and mercury. All results must be below the ICH Q3D Guideline limits before a lot is released.

Synthesized in Switzerland.
Verified by everyone.

Our cGMP-certified synthesis facility in Basel operates under continuous quality monitoring. Every batch is documented from reagent intake through final lyophilization — full chain of custody for every vial you receive.

Our partnership with Eurofins Scientific — one of the world's largest and most trusted analytical testing networks — means results come from a lab with no commercial incentive to pass your product.

Production
cGMP · Basel, CH
Verification
5-point protocol
Response time
<10 min · 24/7
Endotoxin limit
< 0.05 EU/mg

White papers
& publications.

Every formulation in the Zenova catalogue has a published research basis. These white papers summarize the key studies, dosing data, and mechanistic rationale behind each compound class.

Research · 2025 · Recovery
BPC-157 Analogs in Connective Tissue Repair: A Comparative Analysis of Stabilized Variants
A systematic review of pharmacokinetic data comparing standard BPC-157 formulations against stabilized analogs. Analysis of tissue penetration efficiency, half-life, and receptor binding affinity across five independent studies.
Read paper →
Research · 2024 · GLP-1
GLP-1 Receptor Agonist Peptides: Mechanisms of Action in Metabolic Regulation
Detailed mechanistic overview of GLP-1 receptor signalling pathways, covering insulin secretion modulation, gastric emptying effects, and satiety signalling. Includes dosing ranges from published human studies (non-therapeutic context).
Read paper →
Methods · 2024 · Quality
Endotoxin Testing in Research Peptides: Why LAL Assays Matter and What Most Vendors Skip
An explainer on the clinical significance of endotoxin contamination in peptide preparations, the standard LAL assay methodology, and a comparison of endotoxin limits across regulatory frameworks (USP, EP, ICH Q3D).
Read paper →

Independent labs.
No conflict of interest.

Our testing partners are selected specifically because they have no commercial relationship with us beyond the testing contract. They have no incentive to pass a product that shouldn't pass.

01 · Primary Partner

Eurofins Scientific

Hamburg, Germany

One of the world's largest analytical testing groups. Performs our HPLC-MS identity confirmation, RP-HPLC purity, UV potency, and LAL endotoxin assays. No commercial relationship beyond per-test billing.

ISO 17025 GLP Certified USP Compliant
02 · Heavy Metals

SGS Group

Geneva, Switzerland

Our ICP-MS heavy metals screening is conducted by SGS, the world's largest inspection, verification, testing, and certification company. Screens for Pb, As, Cd, and Hg against ICH Q3D limits.

ISO 17025 ICH Q3D Accredited
03 · Sterility

Charles River Labs

Montreal, Canada

Select lots intended for Canadian research distribution undergo additional sterility testing via Charles River. Brings Health Canada-aligned standards to our North American fulfilment stream.

ISO 17025 Health Canada GMP

Letters from the lab.

A monthly dispatch on protocol design, new research, and the occasional behind-the-scenes from our Basel facility. No marketing — just what we'd actually want to read.

~ One letter a month. Unsubscribe in one click. ~