Analytical Services for Drug Formulation
Our analytical services and expertise can support with the quality, safety and efficacy of your drug formulation.
Ensuring excipient compatibility is an important aspect of any drug formulation process. Also factors such as particle size, polymorphism, pH stability and pH solubility to name a few can influence active ingredient bioavailability and hence drug activity.
We can help underpin the quality, safety and efficacy of your new drug formulation by providing services that will be suitable for use in supporting your clinical trials and regulatory submissions.
Our dedicated and knowledgeable analysts have the expertise, capability, techniques and equipment to support a wide range of formulation types throughout the drug development lifecycle from early phase to finished product release and import testing. This includes comprehensive, phase-appropriate analytical method development for both the active pharmaceutical ingredient (API) and the drug undergoing development.
Analytical Services include:-
Other pharmaceutical services