Our experience with a wide variety of novel drug products paired with our flexible cleanroom space may be the solution for your challenging formulation process. If your product cannot be sterile filtered or terminally sterilized, we can develop and validate an aseptic compounding process in our dedicated ISO 5 or Grade A aseptic formulation suites. Our highly skilled engineers will work diligently to fully understand your complex parenteral formulation, important timelines, and will then develop a unique program for you to take your customized process from the bench to GMP. LSNE’s complex sterile formulation services include:
Tangential Flow Filtration (TFF)
Diafiltration
Microfluidization/High Pressure Homogenization
Aseptic Ball Milling
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Client Success Team (CRM),
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