At ResearchDx, our fully accredited and licensed clinical laboratory performs non-clinical and preclinical testing, as well as provides GLP compliance consulting services. For preclinical development programs, we employ a variety of screening technologies to fit your needs. Schedule a consultation with our research team to discuss your specific needs.
Popular options for establishing a biological baseline include:
- Customized evaluation of enzyme activity and inhibition
- Inhibitor screening and validation
- Drug compound detection
- Investigations on the reversibility of enzyme inhibition
- Substrate profiling analyzing the selectivity of enzymes and other proteins
- NGS panel, exome, and whole-genome analysis
- Transcriptome analysis
- DNA sequencing
- Multiplex qPCR panels
Good Laboratory Practices
Our Quality System is maintained to ensure uniformity, consistency, reliability reproducibility, quality, and integrity for all clinical and non-clinical testing. All laboratory studies are planned, performed, monitored, recorded, reported, and archived to ensure traceable data integrity.
GLP Compliance Practices
We comply with Title 21 of the Food and Drug Administration, Department of Health and Human Services, Part 58 regulations for Good Laboratory Practices.
ResearchDx also maintains licensure, accreditation, certification, and/or compliance where applicable to pertinent regulatory bodies and to local, state, and federal laws.
Our CAP/CLIA certified lab, PacificDx offers state-of-the-art facilities and expertise to meet your immediate clinical and pre-clinical needs for high-quality clinical and biopharmaceutical testing services.
Schedule a consultation with our research team today.