USAManufacturedPeptidesFor Provider Confidence

Peptides backed by rigorous testing. Manufactured in the USA with globally sourced ingredients.

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  • ISO 17025Accredited certification

  • Third-party COAFor every product

  • IndependentTesting you can review

BuiltforScrutiny.ARobustCertificateofAnalysis

Everyproductundergoesanintensivetestingpanelthatyoucanviewsoyoucanhavepeaceofmind.

Clinician reviewing peptide quality

Illustrative sample, not a shipped batch

Frontier Biomed LLC429 S. Main StreetRochester, MI 48307

Info@frontierbiomed.comLinkedIn

Sample certificate of analysis

Compound
CJC-1295 No DAC / Ipamorelin
Lot number
Sample
Manufacture date
Sample
Expiration
Sample
Third-party lab
Sample
Chain of custody ref
Sample
AttributeMethodSpecResult
PURITY (HPLC)HPLC-UV>99.0%≥99%
PURITY (MS)LC-MSCONFIRMEDCONFIRMED
ENDOTOXINUSP <85><0.1 EU/mg<0.1 EU/mg
STERILITYUSP <71>PASSPASS

Sample layout for CJC-1295 No DAC / Ipamorelin. This is not a certificate for a shipped batch.

Sample

Not a batch record

Sample

Sample

Frontier Biomed LLC | ISO 13485:2016 Certified | www.frontierbiomed.com

  • Heavy metals

    Verifies heavy metals fall within specified limits.

  • Sterility & endotoxin

    Verifies sterility and endotoxin fall within specified limits.

  • Mass Spectrometry

    Verifies peptide identity by its molecular mass.

  • Purity & Content

    Verifies purity and peptide content meet specified limits.

  • Residual solvents

    Verifies manufacturing solvents fall within specified limits.

Quality Manufacturing Process

STEP 01Sourcing

Sourcing & Raw Material Testing

Raw materials are tested for toxins, heavy metals, and purity before they enter production.

STEP 02Preparation

Preparation & Sterilization

Raw materials are sterilized and prepared into compounds for the lyophilization process.

STEP 03Manufacturing

Manufacturing & Freeze-Drying

Finished products are manufactured in the USA with globally sourced ingredients, freeze-dried, and sent to our seal crimp division.

STEP 04Quality

Quality & Safety Testing

Each batch undergoes a 14-day testing process for endotoxins, mold, bacteria, and metals.

STEP 05Shipping

Secure Shipping

Once testing is complete, products are securely packaged and shipped to you via standard or overnight delivery.

Open Frontier presentation box of 10mg vials beside a single vial

ManufacturedintheUSAwithgloballysourcedingredients

EnsuringNoContamination

  • Heavy metals
  • Toxins
  • Impurities

A Complete System
to Support Providers

Frontier clinicianFrontier team memberFrontier lab scientistOur team has worked in the field since 2016

  • Macro view of a purified peptide solution99% Purity
  • Vials moving through a filling lineManufactured in the USA with globally sourced ingredients
  • Frontier ordering dashboard on a phoneManage all your orders
  • Clinician in a medical facilityVial manufactured in the USA with globally sourced ingredients
  • Technician loading samples into an analyserDigital COAs
  • Sealed Frontier shipping box with tamper tapeSecure Shipping
  • Scientist preparing a sample at a microscopeThird-party tested

One provider platform for sourcing and support.

Frontier Biomed LLC429 S Main Street, Rochester, MI 48307info@frontierbiomed.com

© 2026 Frontier Biomed LLC

Frontier Biomed Labs supplies research-grade chemicals exclusively to licensed healthcare professionals and qualified research institutions for investigational and laboratory research applications. All products are intended for licensed research use only. Frontier Biomed Labs is not a compounding pharmacy (503A) or outsourcing facility (503B) as defined under the Federal Food, Drug, and Cosmetic Act. The ordering provider or institution assumes full responsibility for all regulatory compliance, clinical decision-making, and appropriate use within the scope of their professional license.