Triclinic labs

Triclinic Labs: Comprehensive Materials Characterization and Testing Services

Triclinic Labs is a leading provider of comprehensive materials characterization and testing services for a wide range of industries. With years of experience in the field, Triclinic Labs has established itself as a trusted partner for companies looking to optimize their product development processes, ensure regulatory compliance, and improve overall quality control.

At Triclinic Labs, we specialize in solid form screening and selection, complete cGMP / non-cGMP testing of organics and inorganics, as well as Schedule I-V Controlled Substances. Our state-of-the-art facilities are equipped with the latest technologies and staffed by highly trained professionals who are dedicated to delivering accurate results on time.

Solid Form Screening and Selection

Solid form screening is an essential step in drug development that involves identifying the most stable polymorphs or crystal forms of a compound. At Triclinic Labs, we use advanced techniques such as X-ray powder diffraction (XRPD), thermal analysis (DSC/TGA), microscopy (SEM/OM), and spectroscopy (FTIR/Raman) to determine the optimal solid form for your compound.

Our team has extensive experience working with a variety of compounds including small molecules, peptides/proteins, salts/co-crystals/polymorphs/hydrates/solvates/amorphous forms. We can also provide support for patent applications by generating data packages that demonstrate polymorphic diversity or uniqueness.

Complete cGMP / Non-cGMP Testing

Whether you need cGMP-compliant testing for regulatory submissions or non-GMP testing for research purposes, Triclinic Labs has you covered. Our analytical services include method development/validation/transfer/optimization/stability studies/release testing/degradation studies/impurity profiling/particle size analysis/dissolution profiling/microbial limits tests/endotoxin tests/heavy metals tests/residual solvents tests/water content determination/cleaning validation etc.

We have extensive experience working with various dosage forms including tablets/capsules/injectables/topicals/inhalation products/nanoparticles/liposomes/microemulsions etc., as well as raw materials/excipients/packaging components/environmental samples/waste streams etc. We can also provide support for process optimization by identifying critical quality attributes (CQAs) or critical process parameters (CPPs).

Schedule I-V Controlled Substances

Triclinic Labs is licensed by the Drug Enforcement Administration (DEA) to handle Schedule I-V controlled substances such as opioids/stimulants/depressants/hallucinogens/cannabinoids/synthetic cannabinoids/synthetic cathinones etc. We have strict security protocols in place to ensure compliance with all applicable regulations regarding handling/storage/disposal/reporting/tracking/shipping/etc.

Our analytical services include identification/purity/dosage/formulation/testing/etc., using validated methods that meet DEA requirements. We can also provide support for forensic investigations by analyzing seized drugs/evidence samples/etc., using advanced techniques such as mass spectrometry/gas chromatography/high-performance liquid chromatography/etc.

Conclusion

In conclusion, Trilcininc labs offers comprehensive materials characterization services which includes solid form screening & selection; complete cGMP/non-cGMP testing; schedule I-V controlled substances among others which makes it one-stop-shop solution provider across various industries like pharmaceuticals/biotech/agrochemicals/polymers/material science/consumer goods/oil & gas/mining/environmental monitoring/etc.. With our state-of-the-art facilities equipped with latest technologies & highly trained professionals dedicated towards delivering accurate results on time makes us stand out from other competitors in this industry sector making us preferred choice among clients worldwide!