QC and R&D Services

Ensure product quality and regulatory compliance with robust early-stage analytical method development and validation for finished products, active substances and excipients.

Deconstruction and analysis of proprietary drugs to identify and quantify their components and manufacturing methods, facilitating the development of competitive generic equivalents.

Ensure product quality with our comprehensive testing services. We help you meet regulatory standards, identify potential issues, optimize sourcing, and reduce costs.

Ensuring Data Integrity and Regulatory Compliance LabSense offers comprehensive analytical testing services for clinical trials and BA/BE studies, adhering to GCLP standards. Our services include method development, bioanalysis, pharmacokinetic studies, stability testing, and quality control.

Rheological analysis, using instruments like viscometers, is essential for optimizing drug formulations. It helps ensure product quality, consistency, and effective drug delivery.

In-vitro permeation testing to evaluate drug delivery into the various skin/eye layers and to select formulations for topical and transdermal application. To assess medication transport into the different layers and choose formulations for topical and transdermal use, in-vitro permeation testing is used.

Automated dissolution testing with different apparatus types, methods, automation levels and test setups to determine the most robust method.

Cutting-edge dermal open flow microperfusion (dOFM) testing, an advanced solution for assessing topical drug penetration and bioequivalence. This innovative technology provides accurate pharmacokinetic data directly from the skin, eliminating the need for traditional clinical endpoint studies. Ideal for both hydrophilic and lipophilic substances, dOFM delivers precise and reliable results, accelerating the development process while reducing costs. Unlock the potential of efficient and targeted topical drug testing with dOFM.