Open Communication Crucial in Reassembly and Automation of Process Installation for Laboratoria Smeets
Large scale projects do not always exceed the deadline, budget and the stress limitation of the people involved.
Laboratoria Smeets is a Belgian company with more than 30 years of experience in contract manufacturing and contract packing activities for pharmaceutical and para-pharmaceutical products.
You have successfully submitted your enquiry. Someone from our company will respond ASAP
Laboratoria Smeets is a Belgian company with more than 30 years of experience in contract manufacturing and contract packing activities for pharmaceutical and para-pharmaceutical products.
The company is located near Antwerp on a site that totals 4,200m². All of the company’s production and packing activities are performed under current good manufacturing practice (cGMP) conditions.
Laboratoria Smeets has developed, in collaboration with Ghent University, a technique to produce water-soluble granules containing poorly water soluble drugs of Class II (poorly soluble, highly permeable) or Class IV (poorly soluble, poorly permeable) of the Bio Classification System (BCS).
The faster release of the active pharmaceutical ingredients (API) often results in an improved bioavailability and consequently a decreased intake of API to obtain the same clinical effect.
Laboratoria Smeets’ core capabilities are powder formulation and mixing; liquid formulation and mixing; and packaging of liquids and powders.
The company’s core end-products are sachets of powders, liquids, and tablets; containers (glass and plastic) of liquids and powders; and the filling of powders in bags.
Its goals are:
As part of our contract manufacturing services, Laboratoria Smeets can perform mixing activities for powders and liquids.
Laboratoria Smeets offers contract packing of pharmaceutical powders and liquids, including the following services:
Laboratoria Smeets can provide the following contract services:
A quality assurance (QA) system has been established to regulate all quality-related systems, methods and procedures.
All GMP topics are implemented by way of standards of practice (SOP). A GMP certificate (FAGG), a related production licence, and site master files are available.
QA is responsible for the coordination of the quality system. The qualified person is responsible for the release of the finished products.
Large scale projects do not always exceed the deadline, budget and the stress limitation of the people involved.
API solubility and bioavailability, new technology for pharmaceutical products, twin screw technology, melt granulation and kneading and conveying, etc ... are all topics that are covered in this white paper.
EKICART® is a patented nutraceutical for maintaining healthy joints and to support flexible movement.
Labo Smeets has developed, in collaboration with Ghent University, a technique to produce water-soluble granules containing poorly water soluble drugs of Class II (poorly soluble, highly permeable) or Class IV (poorly soluble, poorly permeable) of the Bio Classification System (BCS). T