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The manufacturing and packaging of pharmaceutical product is highly regulated. At CXV Global, we have a deep understanding of the processes and challenges occurring in the industry. For over 30 years, CXV Global have been assisting pharmaceutical manufacturers who face significant challenges in advancing product quality and still meeting the demands of growing the bottom line and overall business profitability. A case in point is our innovative 360 Degree Bottle and Vial Inspection System specifically designed for the pharmaceutical industry.
CXV Global is an ideal partner to help pharmaceutical manufacturers design and develop products that meet industry connectivity and interoperability requirements and standards. Our solutions and services are geared towards reducing development costs, improving time to market, and reducing the barriers to market entry.
Our solutions comprise of machine vision inspection, vial and blister inspection, vial counting, robotics, serialisation, line clearance assistance, digitalisation and resourcing. Our solutions provide compliance with industry regulations including the Falsified Medicines Directive, FDA CFR 21 Part 11 and GAMP standards.
CXV Global has played a key role in helping our clients succeed in all aspects of the Pharmaceutical Industry from Drug Discovery and Research & Development to Pre-Clinical & Clinical Operations to Automated Manufacturing and Packaging / Supply Chain, including Regulatory and GXP Compliance.
The inspection of pharmaceutical products and packaging to ensure patient safety is a critical quality control function. Machine vision technology delivers standards of resolution, speed and repeatability not possible with manual visual inspection.
Using patent pending technology to reduce line changeover times is the single greatest potential for improving line availability: entire shifts worth of availability can be unlocked by deploying a machine vision system that conducts inspections in milliseconds that would normally take operators minutes.
The CXV Global SmartFactory LineClearance Assistant (LCA) is a machine vision system which assesses the line clearance during line changeovers through objective electronic decisions that are quicker to achieve and repeatable when compared with manual line clearance procedures.
Project Resourcing
CXV Global provides a specific engineering resource, or alternatively, a cross-functional engineering team.
Managed Service Provision
Insource CXV Global expertise to take responsibility for productivity, compliance and quality while operating under client SOPs, KPIs and final approval. The client has visibility and control as CXV Global staff carry out the work.
Functional Service Provision
CXV Global manage the delivery of a function to the pharmaceutical manufacturer customer using CXV Global people to deliver and manage the agreed customers goals. You the customer own the assets – CXV Global fully manages them for you.
The pharmaceutical industry is secured globally through a complex network of regulations. From research and patent applications to packaging and prescribing, each stage in a drug’s life cycle requires compliance with an associated regulation. We support compliance with constantly evolving regulations, from GAMP to anti-counterfeiting.
We’ve been leading the way in the solutions we bring to customer problems and in the deployment of leading edge technologies for over 30 years.
