Pharmaceutical Development & Manufacturing Services

THE GLOBAL SOLUTION FOR THE MANAGEMENT OF CLINICAL SUPPLIES

Fact: 18 out of the top 20 pharmaceutical companies trust CTS with their clinical supplies. Smaller pharmaceutical companies, Biotechs, CROs, Academic Institutions and Government Bodies make up an increasing proportion of the work managed by CTS. We have no minimum study size.

Our wide range of equipment and procedures enables us to manage clinical trial supplies efficiently for everything from the smallest Phase I through to the largest Phase IV clinical trial.

CTS has a successful track record of on-time delivery to the highest quality standards, as demonstrated by our exceptional levels of repeat business.

We are in the unique position of having our sites in both the EU and US inspected by European Regulators and determined to be in compliance with GMP. This simplifies the QP release of clinical supplies for use in trials in the EU, while giving our clients greater choice over where packaging is performed. Our US facilities have also been inspected by the FDA.

CTS is further differentiated by our common ownership with ICTI, a leading provider of IVR and EDC systems for clinical trial management. This enables us to offer a unique package of joint project management services under our EZ-Link banner. Click here to see the full range of benefits of this approach.

Our web-based patient randomisation system WebEZ offers a simple, low cost approach to patient randomisation and drug supply management. Click here for details.