First time in Human – FAST

Pharmaterials have a very responsive team that can work intensively on your API to ensure that the correct decisions are made to get into man as rapidly as possible.

We can start with API optimisation – salt selection and polymorphism, and progress through simple or more complex formulation in order to be sure that the clinical supplies will have the desired properties.

Analytical development and stability testing will be progressed to the appropriate stage for early trial materials.

We will then use the same staff that developed the formulation to run the manufacturing campaign in our cGMP building.

Whether you wish to deliver by the oral route or by inhalation (and potentially other routes of delivery) we can assist.

Please contact us for further details of our high quality rapid pharmaceutical development processes.