We provide services beginning with the consultation, design of your custom-made test, continuing on to development, validation and registration, and then commercialization.
A typical co-development program will involve a 12-24 month timescale and will work as follows:
The Project progress is constantly monitored and reported throughout the entire course of a project. All assay development projects are performed under the rules of ISO and if requested according to IVD regulations. Assay validation can be additionally performed following GLP guidelines.
Our project managers’ disciplined approach to planning, organizing, and managing resources to bring about the successful completion of your specific project goals and objectives allows us to complete your project on time and on budget. Our dedicated project management staff will complete your project in a professional and efficient manner.