Quality Assurance

Quality at Every Stage

Frequency+ operates with structured quality systems to ensure consistency, control, and traceability across sourcing, handling, and distribution.

All relevant documentation, including COAs and product data, is available upon request. For audits or additional documentation, contact our quality team.

Analytical Verification & Traceability

Analytical verification, batch traceability, and documented quality processes across every stage.

01

HPLC Analysis

Assesses purity and impurity profiles across batches.

02

Mass Spectrometry

Confirms molecular weight and structural identity.

03

Batch Traceability

Lot-based tracking across all production stages.

04

Certificates of Analysis (COAs)

Batch-specific documentation with verified data.

GMP & ISO Compliance

GMP Compliance

GMP-compliant manufacturing aligned with ICH Q7 guidelines.

ISO 9001:2015

Certified quality management system ensuring consistent product standards.

Export & Documentation

Full documentation support for international shipments and regulatory requirements.

Manufacturing Facility

Manufacturing & Storage Infrastructure

Our state-of-the-art facility is purpose-built for peptide synthesis and manufacturing, equipped with advanced instrumentation and climate-controlled environments to ensure product integrity at every stage.

Cleanroom Manufacturing

Controlled environments for peptide synthesis and packaging.

Cold Chain Storage

Temperature- controlled storage with continuous monitoring.

Documentation & Verification

Third-Party Testing

Independent verification by accredited laboratories.

Documentation & Audit Support

Complete documentation packages and audit readiness support.

Research Peptide Catalog

Complete specifications and product overview. Detailed documentation available upon request.