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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 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.
