Define the right scope
Clarify the scientific question, available material, timeline, evidence requirements, and constraints before laboratory work begins.

Triclinic Labs helps pharmaceutical and specialty chemical companies solve difficult materials problems through solid-state development, physical and analytical chemistry, advanced characterization, cGMP laboratory services, and chemical intellectual property support.
Clients engage Triclinic when they need answers rather than reports. We work with development, quality, regulatory, manufacturing, and technical teams to explain the behavior of molecules and materials, characterize complex samples, and identify the information needed to move projects forward.
From drug substances and drug products to contaminants, counterfeit materials, and specialty chemicals, we transform analytical data into clear, actionable scientific guidance. That approach has resulted in a 98.3% client repeat rate.
Complex materials problems do not always arrive with an obvious service category or test plan. Start with the decision your team needs to make. A Triclinic scientist will translate that decision into a focused study, coordinate the right capabilities, and adapt the work as the evidence develops.
Clarify the scientific question, available material, timeline, evidence requirements, and constraints before laboratory work begins.
Combine fit-for-purpose methods and expert interpretation so results support one another instead of becoming a collection of disconnected reports.
Receive clear conclusions, practical recommendations, and direct access to the scientists who understand the work and its implications.

Route polymorph, salt, cocrystal, amorphous-form, crystallization, habit, morphology, and manufacturing questions to studies that clarify form selection and control.
Open pageUse MicroED, single-crystal X-ray diffraction, NMR, LC/MS, and related tools to resolve molecular or crystal-structure questions when routine characterization is not enough.
Open pageInvestigate unknown particles, foreign material, impurities, counterfeit concerns, trace-level residues, and quality failures with an identification and root-cause-focused workflow.
Open pageAccess regulated analytical support for XRPD, NMR, particle size, thermal analysis, Raman/FTIR, morphology, release testing, compendial testing, and USP <901> talc testing.
Open pageCompare instruments and techniques by analytical question so your team can choose the right evidence for solid-state, chemical, particle, or materials decisions.
Open pageDevelop, validate, transfer, or troubleshoot fit-for-purpose and cGMP analytical methods for release testing, characterization, and product lifecycle support.
Open pageConnect solid-state, analytical, and formulation evidence to patent, Paragraph IV, prior-art, infringement, validity, and expert-support questions.
Open pageTriclinic Labs can help define the right analytical approach, development path, or next experiment for your specific project goals. Consultations with a scientific subject matter expert are always complimentary