Performs quality control and ensuring the safety and efficacy of drugs by measuring the optical rotation of chiral compounds

Characterizes nanoscale structures in drug delivery systems, including nanoparticles, liposomes, and emulsions. Supports formulation development, stability studies, and performance optimization.

Litesizer DLS delivers precise particle size analysis using advanced Dynamic Light Scattering technology, enabling accurate characterization of nanoparticles, emulsions, and suspensions to optimize stability and performance in drug delivery systems.

Accelerates oxidative stability testing, essential for evaluating the shelf life and stability of APIs and drug formulations sensitive to oxidation.

Measures the particle density and porosity of powders and granules, crucial for optimizing formulations in tablets and controlled-release systems.

Measures pore size distribution and porosity of pharmaceutical materials using mercury intrusion porosimetry. Supports formulation performance, quality control, and batch consistency.

Laser diffraction technology delivers accurate and reproducible particle size distribution analysis for powders, granules, and suspensions, supporting pharmaceutical formulation development, quality control, and regulatory compliance.

Raman spectrometer for identifying chemical components in raw materials and finished products, ensuring quality and compliance in drug formulations.

Used for fast, efficient sample digestion, enabling precise trace element analysis and ensuring pharmacopeia compliance in raw materials and APIs.

Monitors polymorphism, crystallinity, and phase transitions of APIs and formulations using real-time X-ray diffraction. Supports pharmaceutical development, stability studies, and quality assurance.

The new MCR Series delivers precise rheological characterization of pharmaceutical formulations, including gels, creams, suspensions, and injectables, enabling optimized stability, texture, processability, and quality control throughout drug development and manufacturing.

Measures surface area and pore size distribution of pharmaceutical powders for excipient characterization, formulation development, and quality control.

Measures surface area of APIs and excipient to determine their porosity and dissolution behavior

Performs thermal analysis to support pharmaceutical quality control by measuring melting behavior, crystallinity, polymorphism, and stability of APIs and formulations, ensuring safety, efficacy, and regulatory compliance.

Precise viscosity measurements, critical for controlling consistency in liquid formulations, syrups, and semi-solids.

Measures viscosity in small volumes, ideal for injectable solutions, and anti-cancer drugs