In the pharmaceutical industry, processing instrumentation is within environments that are shaped from the FDA, GMP, and other organizations regulations. TriNova Inc. understands the challenges the pharmaceutical industry faces in terms of developing and distributing products in a safe and efficient way.
The pharmaceutical industry is a global industry which faces many aspects. The most important of them is the respect of the key regulations of GMP. GMP facilities are permanently improving their level of compliance. Moreover, GMP manufacturers work with GMP partners. This is the reason TriNova Inc. has implemented its own compliant strategy consisting of creating a Corporate Team dedicated to the implementation of a Validation Master Plan and executing and monitoring the specified actions. The new “theory of growth” considers the innovation as a process which contributes to driving the economic development. The constraints of the market (regulation, laws, total quality, procedures, traceability as examples) are day after day increasingly stringent and costly to implement in a very short time.
PHARMACEUTICAL GRADE INSTRUMENTATION EQUIPMENT
Pharmaceutical companies utilize pumps to process, dose, mix or transfer medicine or final products. TriNova’s instrumentation equipment can meet any sanitary and safety requirements for your pharmaceutical processes. We can assist with selecting pharmaceutical instrumentation equipment and offer manufacturing brands that are known for clean, effective, and safe products.
PROCESSING EQUIPMENT FOR THE PHARMACEUTICAL INDUSTRY
There are many product branches where our pharmaceutical processing products are installed. Some common applications for TriNova’s processing equipment include: