Companies specializing in dispersion, mixing and the milling of solids as components of liquids have adopted state-of-the-art and dedicated cleanroom settings for meeting the standards prescribed in what’s known as GMP, or good manufacturing processes.
Such implementation of practices involves stringent operating guidelines and consistent documentation of every process, from room and tool cleaning to equipment sanitation, to meet with customers’ high-level requirements.
What Are Good Manufacturing Practices?
GMP processing is based on standards prescribing the consistent production and control of goods according to process-quality requirements. These standards are called GMP, or good manufacturing practice, per the US Food and Drug Administration, which legally require processors, packagers and manufacturers of medical devices, food, drugs or blood to take steps ensuring effective, pure and safe products.
GMP in Dispersion Technology
GMP processing at dispersion technology providers, including providers of dispersion, mixing and milling equipment and tool processing services, employ dispersion experts that can assist in all production steps, including product formulation, piloting test batches, small-scale production runs and packaging.
GMP-Related Services
Analytical labs have all necessary equipment for product-quality confirmation and the provision of complete certificates of authenticity. These services include:
- Class ISO 8/100,000 cleanrooms
- Half-gallon to 300-gallon batch sizes
- Dust filtration systems
- Climate controlled environments
- Water system heating or cooling for temperature sensitive processes
- Food grade processing equipment
- Room pressurization with HEPA filtration systems, ensuring consistently flowing clean air
GMP serves to remind manufacturers to employ up-to-date systems and technologies to meet with current regulations. The objective is to prevent mixups, contamination or errors that may have appeared historically, and toll milling companies with regulation cleanrooms and equipment can provide the necessary means for maintaining GMP processing standards.
