VxP Pharma Formulation Services
Drug candidates can present specific challenges such as low bioavailability, poor solubility and unreliable physical stability. At VxP, we understand that formulation development is as much an art as it is a science. Our formulation team includes PhD and M.S level formulators with decades of industry experience, and no matter what type of challenges you are facing, there’s a good chance we’ve worked on something similar.
Our top priority is providing a safe, robust, and scalable form of delivery, and the most viable manufacturing strategy for your drug candidate.
Formulation development for new chemical (NCE) and new biological (NBE) entities
Optimization of existing formulations
Process development for specific dosage forms
Improving delivery of existing dosage forms
Developing controlled release, sustained release, and complex formulations
Dedicated suites for the handling of DEA Scheduled Compounds, as well as suites for Cytotoxic and Potent Compounds
Our team can offer complete guidance, including from a regulatory standpoint, for the development and manufacturing of your compound. We have a comprehensive and full-service operation for clinical trial materials preparation in support of Phase I – III development as well as for commercial scale-up. Our services are cGMP compliant and include established protocols, efficient documentation practices, and effective QA management. We can be your greatest resource.
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