THE SOVEREIGN STANDARD
Institutional standard for Peptide validation.
Providing forensic-grade analytical clarity for the world's leading Pharmaceutical innovators through immutable verification protocols.
Sectors We Support.
Peptide Manufacturers
Independent batch-to-batch verification to ensure yield and purity targets are met before distribution.
Pharma & Biotech R&D
Technical support for early-stage discovery and preclinical stability studies with full instrumentation access.
503A/503B Pharmacies
Sterility, potency, and endotoxin verification for compounded sterile preparations (CSPs).
INSTITUTIONAL INTEGRITY
A Trusted U.S. Pharmaceutical Lab Entering the Peptide Vertical.
Established in 2010, Capzer started with a singular mission: to provide high-stakes analytical data for pharmaceutical manufacturers who cannot afford ambiguity.
Unlike consumer-facing "testing platforms" that outsource their lab work, we are a physical, brick-and-mortar facility in Lake Worth, FL. We maintain a zero-conflict integrity mission, ensuring that our results are purely empirical—shielded from commercial interests and built for regulatory scrutiny.
2010
Laboratory Founding
100%
US-Based Operations
Facility Compliance & Regulatory Anchors
CLIA/COLA Standard Operating Procedures
Our internal protocols mirror clinical diagnostic rigor, ensuring the highest reproducibility in the industry.
DEA Schedule I-V Handling
Full licensure for the analytical handling of controlled substances for research purposes.
HIPAA-Grade Data Security
All intellectual property and formulation data is stored on encrypted, air-gapped local servers.
FACILITY STATUS
Active & Inspected 2024
THE STANDARD OF INTEGRITY
Permanence in Every Molecule.
Cryptographic Hashing
Every COA is processed through our SHA-256 ledger, ensuring that once a purity report is issued, it can never be altered or retracted.
Temporal Auditing
Track the chronological history of any batch from synthesis to sovereign storage with 100% data fidelity.
Decentralized Backups
Data is distributed across high-security nodes globally, preventing single-point failure and ensuring 99.99% archival uptime.
LIVE INTEGRITY STREAM
BATCH_ID
#CC-TB-500-A2
PURITY_INDEX
99.82% [CERTIFIED]
SYNTHESIS_LOCK
100% COMPLETE
BLOCK_HASH: f7e21a...002c91
TIMESTAMP: 14:02:11 UTC
NODE: ZURICH_HQ_01
STATUS: [SOVEREIGN_ARCHIVED]
THE SOVEREIGN STANDARD
Built for Compliance.
Designed for Truth.
"If a batch fails, it fails."
Our independence is our currency. We offer no consultative manufacturing; only cold, hard, defensible analytical data.
01
Purity Testing
HPLC analysis to determine exact peptide concentrations.
02
Identity Confirmation
Mass Spectrometry to ensure molecular weight accuracy.
03
Amino Acid Analysis
Quantitative composition verification of peptide chains.
04
Endotoxin Screening
LAL testing to detect pyrogenic contamination.
05
Sterility Assurance
Microbiological assessment for aseptic confidence.
06
Stability Studies
Accelerated aging and shelf-life determination.
The Verification Workflow
Submit Request
Upload sample specs and select required analytical tests.
Quote & Ship
Receive a transparent quote and shipping instructions within 4 hours.
Forensic Analysis
Our scientists perform multi-stage testing on state-of-the-art equipment.
Receive Ledger
Download your clinical-grade COA from our secure portal.
THE CAPZER DIFFERENCE
Beyond Simple
HPLC Analysis.
01
Multi-Ortho Profiling
We utilize three independent orthogonal methods to verify peptide purity, leaving zero room for chromatographic co-elution errors.
02
High-Res Orbitrap MS
Mass accuracy within 2ppm ensures absolute structural confirmation of the amino acid sequence and modifications.
03
Regulatory-Ready Reporting
Comprehensive data packages designed for direct submission to institutional review boards or regulatory bodies.
LIVE BATCH STATUS
BATCH_IDCP-7742-X
TIMESTAMP2024.10.24 14:02 UTC
ISO_PROTOCOLACC-17025.A
Technical Capabilities
Our laboratory leverages Agilent and Waters instrumentation to deliver sub-decimal precision.
HPLC / UPLC Analysis
Ultra-performance liquid chromatography for high-throughput purity profiling with rapid turnaround.
RESOLUTION
Sub-2μm Particles
SENSITIVITY
LOD < 0.1ppm
LC-MS/MS
Exact mass identification and sequence mapping for absolute structural confirmation.
InstrumentOrbitrap Exploris
IonizationESI+ / ESI-
Safety Testing
- Endotoxin (LAL Method)
- Bioburden / Sterility
- Residual Solvent (GC-MS)
Automated Reporting
& API Integration
Seamlessly pull laboratory data into your inventory management system via our RESTful API.
GET /v1/verification/BTH-492-X
{
"status": "verified",
"purity": 0.9982,
"sequence": "H-His-Ala-Glu-...",
"timestamp": "2024-10-12T08:00:00Z"
}
Frequently Asked Questions
How do you ensure samples aren't cross-contaminated?
+
We utilize dedicated HPLC/UPLC columns for specific peptide classes and employ validated multi-stage cleaning protocols between every run. Our air-flow systems are designed to clinical cleanroom standards to prevent environmental drift.
What is the typical turnaround time for Purity Analysis?
+
Standard turnaround is 3-5 business days. Expedited forensic-grade reporting is available for urgent validation needs, delivering results within 48 hours of sample intake.
Are your COAs accepted for FDA New Drug Applications?
+
Yes. Our analytical data is generated within a DEA-licensed, US-based facility following cGMP-aligned protocols, ensuring full defensibility for IND and NDA submissions.
Do you provide bulk discounts for large peptide vendors?
+
We offer scalable institutional pricing for compounding pharmacies and bulk R&D vendors requiring high-volume recurring validation across multiple peptide lots.
Ready to Verify
Your Peptide Quality?
Join hundreds of labs and manufacturers who trust Capzer for definitive analytical results. Get a custom quote within 4 business hours.
99.8%
ACCURACY RATE
48hr
STANDARD TURNAROUND