The first step in every R&D project to design an adequate research plan that gives you the right answer to your scientific question. The research plan in clinical genomics has of special importance since in this field you may have a limited access to patient samples and for analysis functional genomic techniques are rather expensive.

We have a long-standing experience in design and implementation of clinical genomic studies that forms the basis of UD-GenoMed’s consulting service. The above services we offer not only to our pharma and biotech industrial partners, but also to academical partners.

Depending on your project-specific requirements, we offer:

joint discussions and "brainstorming" about your research plan identification of critical points development of inclusion and exclusion criteria for patient accrual development of logistic plan and timescale of patient recruitment optimization of instruments, material and methods and requirements setup of feasibility studies definition of quality specifications design of biostatistical data analysis training sessions for specific areas of interest

This consultation process leads to an elaborated work plan and a set of recommendations for our customers.

We are also ready to assist in the implementation of your clinical genomic research project from the first clinical samples to data interpretation.

Provided you have further questions, please contact us!