Whether your project involves a greenfield build, retrofit, or upgrade, automation in biopharma and life sciences industry demands three critical pillars:
- Complex, proprietary processes
- Accelerated delivery and speed to market
- Strict regulatory compliance (FDA, EMEA, PMDA)
PACIV’s control systems, information solutions, and instrumentation services are designed to meet these demands, ensuring full compliance with industry standards and timely execution across every phase of your project.
Biopharma and Life Science Automation
PACIV’s founders, directors, and team members bring decades of hands-on experience in the regulated life sciences industry. We understand the critical importance of designing, building, installing, commissioning, validating, and maintaining systems that meet stringent quality and compliance standards.
Our solutions are engineered to uphold the essential process parameters that ensure product Safety, Identity, Strength, Purity, and Potency (SISPQ). We recognize our role in enabling reliable, compliant manufacturing systems that support timely market access and consistent product quality.
Global Expertise. Proven Results. Trusted by Life Sciences Leaders.
PACIV delivers automation and integration solutions tailored to the life sciences industry, with a global presence strategically located near client manufacturing sites. This proximity enables consistent interpretation of corporate automation standards and regulatory guidelines, reducing cost and accelerating delivery of automated systems.
With deep expertise in regulated environments, PACIV supports clients across the full system lifecycle, from design and implementation to optimization and support.
Our team identifies process improvements, selects the right technologies, and ensures compliance with industry standards, driving operational excellence and maximizing value from both new and existing manufacturing assets.
