IMS SRL cooperates with the leading manufacturers of active ingredients and finished products on the European and Non – European countries, adopting specific business strategy
In order to achieve the improvement of its quality standards, the company is periodically inspected by the Italian Drug Agency (AIFA) and by the Food and Drug Administration (FDA).
IMS is accredited in Japan at PMDA and approved by the Korean Food and Drug Administration (KFDA) Administration.
The company is also ISO 9001:2015 certified.
IMS offers integrated services in the treatment of APIs in accordance with the GMP requirements
Production processes guarantee particles size even to values less than 5 μm with the possibility of using air or nitrogen as process fluid.
The analyzes conducted with the use of laser technology guarantee the compliance of the micronized product with the requirements of bioavailability and pharmaceutical technique.