99.6% purity
Lean mass research protocol
Bulking X
$150
- Ipamorelin15 mg
- GHRP-610 mg
- Follistatin10 mg
Subcutaneous pen · Made in Germany
Request datasheetISO 9001 · GMP-Aligned Facility
Advanced peptides,
engineered for science.
Aura BioLabs manufactures high-purity peptide research solutions with pharmaceutical-grade quality control, third-party validated analytics and complete batch traceability.
ISO 9001:2015
GMP Aligned
HPLC Verified
Mass Spectrometry
COA Every Batch
Third-Party Audited
Product authenticity
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Product Line
Eight signature protocols.
Precision-formulated by Aura BioLabs for advanced peptide research.
99.5% purity
Contest preparation profile
Pré Contest X
$160
- GHRP-220 mg
- HGH20 mg
Subcutaneous pen · Pharmaceutical grade
Request datasheet99.5% purity
Combined growth & regulation pen
Mix Low
$280
- HGH50 IU
- Follistatin20 IU
Pen injector · Refrigerated storage
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Oral peptide research solution
Peptiva RX
$80
- BPC-157500 mcg
- AOD-9604300 mcg
100 mL oral solution · Citrus berry
Request datasheet99.7% purity
10 mg single dose
RETRATRUTIDA™
$120
- Retratrutide10 mg
- Volume0.5 mL
Prefilled pen · Subcutaneous use only
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Combined peptide research pen
EUROGOLD
$180
- Somatropine20 mg
- Ipamorelin35 mg
- GHRP-628 mg
Prefilled pen · 3 mL solution for injection
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120 mg peptide research pen
Retratrutide 120 mg
$200
- Retratrutide120 mg
Pen injector · 120 mg presentation
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The Science
Four disciplines. One standard of purity.
We treat every peptide as pharmaceutical material — because researchers deserve results they can build on.
Synthesis
Reactor-controlled peptide synthesis with in-process monitoring at every stage of the pathway.
Analytical
HPLC, GC-MS and NMR spectroscopy validate purity, structure and stability of every batch.
Assurance
Independent third-party laboratories confirm identity, potency and absence of contaminants.
Traceability
Every unit is serialized and linked to a full digital audit trail from raw material to shipment.
Aura BioLabs Analytical Lab
Zurich, Switzerland
Quality Control
Every batch. Every unit. Every time.
Our quality framework is modeled after global pharmaceutical standards. Materials are verified across four independent stages before release, and every shipment includes a batch-specific Certificate of Analysis.
- Identity confirmation via NMR and mass spectrometry
- Purity quantification through validated HPLC methods
- Residual solvent and heavy metal screening
- Stability programs for long-term storage integrity
Get in touch
Ready to work with a laboratory partner you can trust?
Request our full catalog, technical datasheets and pricing for research institutions.