The pharmaceutical industry requires its manufacturing processes to satisfy the highest standards for quality, proper sanitation, and dependability. Because they properly manage the flow of fluid, pressure, and temperature during treatment manufacturing, control valves are needed for maintaining these standards. The pharmaceutical industry have to select proper valves for control for maintaining product quality, safety, and compliance due to high regulatory standards and the demand for contamination-free processes.
We are Leading manufacturer of pharmaceutical machinery, UNIMAC CONTROL SYSTEM produces cutting-edge automation and control systems that improve productivity, secure product safety, and satisfy global regulatory demands like Food and Drug Administration, WHO, and GMP. Process automation systems, PLC-based control panels, SCADA systems, VFD panels, and instrumentation solutions designed specifically for pharmaceutical manufacturing facilities are all included in our product range.
List of Challenges in Pharmaceutical Processing with point-wise explanations:
Pharmaceutical processes must meet rigorous standards (FDA, GMP, EMA), requiring extensive validation, documentation, and audits.
Handling APIs, biologics, and hazardous materials requires specialized containment and processing solutions.
Expensive equipment, cleanroom facilities, skilled labor, and validation procedures drive up costs.
Regulations demand secure, accurate, and retrievable electronic data records for all processes and batches.
The pharmaceutical industry requires the control valves industry to supply the accuracy, hygienic conditions, and dependability needed for reliable and secure manufacturing of pharmaceuticals. Control valves properly manage temperature, pressure, and flow—all important variables in activities including water transfer, mixing, and cleaning. Having its easy to use, crevice-free surfaces and hygienic, FDA-compliant materials, these valves offer in maintaining integrity and minimizing an infection.
Our expertise ensures that your operations achieve the highest standards of quality, compliance, and efficiency, driving innovation while maintaining patient safety.
Advanced automation systems to streamline production, reduce human error, and enhance batch consistency.
Innovative platforms and data analytics to accelerate drug development and clinical trials.
End-to-end solutions for inventory management, traceability, and cold chain logistics to ensure product integrity.
Integrated software and monitoring tools to maintain compliance with FDA, EMA, and GMP regulations.