VxP Pharma understands early-stage development challenges, and can provide multiple dosage form options to accelerate your drug development programs.
We understand that each formulation is unique, just as each drug candidate is unique. Certain drug candidates can present specific challenges such as low bioavailability, poor solubility and unreliable physical stability. Our experienced formulation development team can provide seasoned support in overcoming many of these issues. The top priority is providing a safe, robust, and scalable form of delivery and the most viable manufacturing strategy for your drug candidate.
The formulation experts at VxP Pharma can provide you with numerous years of combined experience for every aspect of formulation design. Rather than limiting ourselves to the capabilities of one laboratory, we approach every project by selecting the scientists and groups most appropriate for the type of dosage form desired. With multiple facilities and highly-trained scientists available, we are ready to customize your formulations according to specific requirements, utilizing the site-to-site connectivity and optimizing your resources and processes by combining the talents of the scientists with your team.
At VxP Pharma, the formulation experts provide product development expertise to support many routes of administration:
- Solid dosage formulations
- Semi-solid oral formulations
- Sterile liquid dosage formulations
- Parenterals (intravenous, intramuscular, and subcutaneous)
- Lyophilized formulations
- Topical formulations
VxP Pharma Formulation Services
- 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
- Controlled release, sustained release, complex formulations
The experienced scientists can offer complete guidance for manufacturing practically every dosage form available with strict quality compliance. We have a comprehensive and full-service operation for clinical trial materials preparation in support of Phase I – III development and commercial scale-up. The services are cGMP compliant and include established protocols, efficient documentation practices, and effective QA management.
The state-of-the-art labs are staffed by some of the best trained and most experienced subject matter experts in the field.