Once design, construction and general commissioning are completed, pharmaceutical facilities must be qualified and their processes validated. METO Systems knows the differences, and understands the impact of a qualified facility operating under Good Manufacturing Practices (GMP) regulations.
METO Systems recognizes that equipment provided to the industry must be constructed to a consistent standard to minimize the risks involved in pharmaceutical production. We have built a long and trusted reputation for equipment compliance, providing DQ, IQ, OQ and PQ documentation required for process validation.
The ‘Bright Shop’ at our Franklin Lakes facility and a spacious clean area FAT facility out of Bristol Connecticut to eliminate the chance of contamination during the manufacturing process.
METO Systems is a leading supplier of stainless-steel material handling equipment to the pharmaceutical industry. Every piece of machinery we build is tailored to meet our clients’ needs at every stage of operation throughout the production process.
We produce products that can handle everything from fine powders and particulates, such as those produced during milling, to granulated compounds and large collections of pressed tablets.
Advantages
- Products manufactured under GMP regulations
- Full set of qualification documents provided for validation
- Dependable products customized to meet the rigorous demands of pharmaceutical operations
Questions?
METO Systems material handling and processing equipment can be customized for nearly any application. If you don’t see your specific application listed, contact us at 201-405-0311 or visit our contact us page and one of our engineers will discuss your specific needs and requirements.