Our Quality Commitment
Every aspect of our operations ensures the integrity, purity, and consistency of research materials.
Validated Methods
All analytical methods are validated for specificity, linearity, accuracy, and precision following ICH guidelines before use in production QC.
Batch Documentation
Complete traceability from synthesis through final release. Every batch has documented production records and test results.
Stability Programs
Ongoing stability monitoring ensures products maintain specifications throughout their stated shelf life under recommended storage.
Included with Every Order
Comprehensive documentation supports your research and regulatory requirements.
Certificate of Analysis
Batch-specific purity, identity, and quality data with test dates and acceptance criteria.
HPLC Chromatogram
Purity analysis trace with integration report and method parameters.
Mass Spectrum
Molecular weight verification with observed vs. theoretical comparison.
Safety Data Sheet
Handling, storage, and safety information following GHS classification.
Compliance Standards
Our policies ensure responsible conduct in all research and commercial activities.
Customer Qualification
- Verification of research institution or qualified laboratory status
- Agreement to RUO terms and conditions before purchase
- Confirmation of intended research use application
Ethical Standards
- Commitment to responsible research practices
- Transparency in product specifications and limitations
- No promotional claims of therapeutic benefit
Shipping & Handling
- Temperature-controlled shipping for sensitive materials
- Proper hazardous materials documentation when required
- Compliance with applicable shipping regulations
Record Keeping
- Retention of batch records for minimum 5 years
- Customer order history for traceability
- Quality deviation and CAPA documentation
Questions About Our Compliance Standards?
Contact our quality team for detailed information about policies, documentation, or regulatory questions.