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The manufacturing and packaging of pharmaceutical product is highly regulated. At CXV Global, our close proximity to clients has resulted in a deep understanding of the processes and challenges occurring in the industry. A trusted partner, we have been assisting pharmaceutical companies to achieve compliance with regulations since 1986.
Our solutions comprise of design, hardware, software, support and training services and 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.
