Starting with the Target Product Profile, and further refined by Clinical Development Program and technical properties, LFSCNC can support you with determining the most optimal formulation appropriate for use in the intended clinical studies.

 

In addition and given the above, our team at LFSCNC can also assist you with outlining a plan for further development of Drug Substance/Drug Product in accordance with GMP.

 

If required, LFSCNC can project-manage DS/DP development on a day-to-day operational basis in order for your company to monitor progress and ultimately to be able to meet pre-established goals.   

"The manufacturing process and related supply chain for our biotechnology product is very complex. How can we optimise  the current process also in order to develop a formulation/dosage form appropriate for use in the intended clinical studies"

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