About Tru & Co TRU & CO
Pioneering accessible research solutions with pharmaceutical-grade quality.
Our Mission
TRU & CO is a licensed U.S. business entity focused on the supply of research-use materials. The company works exclusively with manufacturers that operate under internationally recognized quality systems, including WHO/GMP alignment and ISO 9001:2015 certification.
All sourcing decisions prioritize documented manufacturing controls, consistency of processes, and adherence to established quality management frameworks. Direct engagement with qualified facilities allows TRU & CO to maintain oversight across the supply chain while offering commercially efficient distribution.
Quality-Driven Operations
TRU & CO provides a structured, secure, and discreet online platform for the distribution of high-purity research peptides. Operational standards emphasize documentation, traceability, and controlled handling at every stage of fulfillment.
Orders are processed promptly within the United States. Customer support is based domestically and available through standard communication channels, including phone and email, to assist with order-related inquiries and logistics.
Our & Core Values
Our commitment to quality is backed by internationally recognized certifications.
Operational Distinctions
Our commitment to excellence is reflected in every aspect of our operations, from manufacturing partnerships to quality verification processes.
Collaboration with FDA-registered manufacturing partners and independent analytical laboratories
Production conducted in facilities operating under GMP-aligned quality systems
Analytical verification of material purity, typically reported at ≥99%
Evaluation for sterility and endotoxin presence based on established laboratory methods
Efficient order processing, including same-day fulfillment where applicable
U.S.-based customer service for operational and order support
Multiple accepted payment methods, including electronic and bank-based options
Our Vision & Quality Certifications
TRU & CO applies a multi-layered quality verification model that extends beyond basic identity and content analysis. Batches are submitted to independent third-party laboratories for additional evaluation, which may include endotoxin screening and sterility assessments performed by laboratories operating under ISO/IEC 17025:2017 accreditation.
These procedures are intended to support research integrity and reduce the risk of material contamination.
Documentation Standards
Each production lot is accompanied by analytical documentation detailing test parameters and results, including purity, identity, and sterility evaluation where applicable.
These controls are integral to TRU & CO's quality governance model and reflect the company's emphasis on transparency and procedural rigor.