Multimilling Station

Production and handling of HPAPI or toxic products (in gas or powder form) need the total product separation from the environment to protect operators. Negative pressure regime is maintained within the closed volume of the isolator. Turbulent flow is generally adopted.
Operator access to isolator inside...

Milling operations may result in dust clouds, exposing operators and environment to HPAPI, due to high energy involved in process operations and size reduction down to few m. Proven solutions are available for laboratory, pilot unit or production units of: •  Conical mills •  Hammer mill •...

Milling operations may result in dust clouds, exposing operators and environment to HPAPI, due to high energy involved in process operations and size reduction down to few m.Proven solutions are available for laboratory, pilot unit or production units of: •  Conical mills •  Hammer mill •  ...

The equipment, designed to be installed across different floors, is composed of a glovebox to discharge the batches from a filter dryer without affecting the product sterility; a jet mill isolator provides a confined environment in which the product is micronized; downflow booths are integrated on the ...

Pack-off systems assure product protection and reduce operator dust exposure during discharging operations from silos, bins, cyclones, driers, reactors, centrifuges, …
It is possible to install pack-off systems on existing equipment, reducing to a minimum the requested modification, in full compl...

Milling operations may result in dust clouds, exposing operators and environment to HPAPI, due to high energy involved in process operations and size reduction down to few μm.
Proven solutions are available for laboratory, pilot unit or production units of:
•  Conical mills •  Hamm...

Containment systems for sterile applications may be proposed in the form of closed isolators or Restricted Access Barrier Systems (RABS).
A sterile isolator allows to avoid the use of sterile cleanrooms, reducing the sterile volume around the process being executed.
Turbulent or unidirectional fl...

Single chamber barrier isolator configured in order to grantthe dispensing procedure for API product achieving the followingtasks:• Assure a sterile environment inside the isolator. Assure operator protection, when the processedproducts are highly active.The barrier isolator operates under a positive ...

PilotMill-Zero represents the right solution for preliminary feasibility micronization trials with milligrams batches of New Chemical Entities, as well as of many other products.
• Based on the proven FPS Spiral Jet Mill technology • Designed to effectively operate despite the miniaturized dimensions ...

The LaboMill/PilotMill-1 is the FPS answer to R&D lab needs when it comes to very initial stages of development, when only extremely small "batch sizes" are available. This very limited amount of material - starting from 200 mg - asks for the use of very special equipment designed and develop...

The R&D QMill isengineered to meet the requirements of R&D labs, where new product are developed and micronization process is requested on small quantities (from minimum 1g to few kgs).
All connections of components are made to be in compliance with cGMPs and to assure quick a...

The PilotMill-2 jet mill is designed for product research and developments needs, where batches from 1g to 3kg are considered. In function of these process condition, the PilotMill-2 jet mill has been designed to assure higher micronized product yield.  It is available in top discharge ...

"We are highly specialised in the design and manufacture of custom isolators for potent active ingredients and sterile solutions. Our collaborative design process includes creating full-scale mock-ups to validate ergonomics and functionality, ensuring tailored solutions for each client." - Paolo Barilli - FPS Pharma Process Engineer

Let's explore the FPS Pharma Engineering Process.

Explore FPS’ micronization and jet milling systems. Achieve exact PSD targets, enhanced bioavailability, and cGMP compliance for superior formulations.