Frontier Biomed

Initializing private research

USAManufacturedPeptides For ResearcherConfidence

Peptides backed by rigorous testing and 99.6% Purity. We create our products in the USA to ensure quality and reliable results you can trust.

  • ISO 17025Accredited certification

  • Lot-levelTraceability on all products

  • COA on arrivalCertificate of Analysis included

BuiltforScrutiny.ARobustCertificateofAnalysis

Everyresearchproductundergoesanintensivetestingpanelthatyoucanviewsoyoucanhavepeaceofmind.

Clinician reviewing research peptide quality

Analytical data for this shipment

Frontier Biomed LLC429 S. Main StreetRochester, MI 48307

Info@frontierbiomed.comLinkedIn

Certificate of Analysis

Compound
CJC-1295 No DAC / Ipamorelin
Lot number
LOT-200501-A
Manufacture date
01 May 2025
Expiration
01 May 2027
Third-party lab
[Lab Name]
Chain of custody ref
CCR-200501
AttributeMethodSpecResult
PURITY (HPLC)HPLC-UV>99.0%≥99.5%
PURITY (MS)LC-MSCONFIRMEDCONFIRMED
ENDOTOXINUSP <85><0.1 EU/mg<0.1 EU/mg
STERILITYUSP <71>PASSPASS

This item is regularly tested by the manufacturer and meets all requirements defined by the appropriate current ingredient specification. This item is manufactured, packaged, stored, and shipped in accordance with good Manufacturing Practices and under modern sanitary conditions.

Benzy Ross

Quality Control Manager

01 May 2024

Verified

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

APIs are sourced from US FDA-certified facilities and tested in our USA facilities for toxins, heavy metals, and raw material purity.

STEP 02Preparation

Preparation & Sterilization

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

STEP 03Manufacturing

Manufacturing & Freeze-Drying

Finished compounds are manufactured in our South Carolina, USA facility, 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 research vials beside a single vial

EvenTheVialsAreManufacturedintheUSA

EnsuringNoContamination

  • Heavy metals
  • Toxins
  • Impurities

A Complete System
to Support Researchers and Providers

Frontier clinicianFrontier researcherFrontier lab scientistTrusted in the field since 2016