We take the challenge
What are your biggest method development and validation challenges? Combining our experience and technical understanding, we develop methods efficiently to create methods suitable for today’s regulatory standards. To make confident decisions on the selection of appropriate analytical techniques and methods, you need a partner with the deep analytical capabilities and validation expertise required to ensure the generation of robust data of unparalleled quality across your organization
Method Development
Method Validation
Reference Materials
Customized QC
OEM/CDMO
Consultation
Formulation & method Development
Our reliable qualitative and quantitative analytical method development includes identification, separation, purification, and quantitative estimation of your compound mixtures.
Method Validation
Verify the analytical method for an intended purpose, ensure methods complying with a variety of industrial committees, competent Authorities, and standards organizations for purposes of quality control and regulatory compliance.
Report your products' selectivity/specificity, precision, accuracy, linearity, Stability, Limit of Detection (LOD) and Limit of Quantitation (LOQ)
Reference Materials
Are you traceable?
Using Reference materials are so critical element of your workflow, starting from formulation, through development of method, calibration, quality control, validation of methods, to commercializing your products.
We help you to select a wide range of certified reference materials (CRMs) and other quality reference materials, to certify your analysis in accordance to NIST, ISO 17034, 17025, ISO 9001 and other metrological organizations.
Customize your QC
We customize your DOA Quality Control “QC” to 100% fit your laboratory and/or your local requirements. We ensure your confidence about your lab results, by offering wide range of analytes selection (single to multiplex), with flexibility to select your ranges and levels (set you cut-offs) for different screening and confirmatory applications (Immunoassay, Gas and liquid chromatography) and different methods (manual & Automation), different Liquid or Lyophilized forms and your choice of selection for vials’ sizes, volume, designs and private labelling.
OEM/CDMO
Accelerate your products commercializing.
We partnership with specialized leaders to offer a complete customized services from development to contract manufacturing to meet production needs for high-quality, controls, calibrators, and reagents, implementing strict Quality Assurance (QA), Quality Control (QC) and Quality Management System (QMS) to ensure that all products/services are aligned with quality standards and regulatory requirements (US FDA, MDSAP, IVDR and any other International Quality Standards like ISO 9001 and ISO 13485).
Consultation
Our consultants have the knowledge and experience to take your ideas or even dreams to tangible through all stages of the project life cycle, from scratch to all the way to commercialization. From project resources, SOPs, QC/QA process, documents writing, to regulatory and conformity registration assessment