Founded in 1990, Campbell Informatics is an integrated services and technology company that provides leading-edge compliance solutions to lifescience manufacturers, suppliers and regulators on a global basis across the total lifecycle.

Our compliance services are lifecycle-driven and include strategic consultancy, commissioning & qualification, data management, quality risk management and people placement, for synthetic and biotech project situations.

Our world class compliance technology enables us to itemize, specify and verify manufacturing systems and processes, precisely, quickly and economically, delivering major cost/time/quality benefits relative to traditional methods.

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Having successfully completed a 12-month risk assessment assignment on behalf of FDA’s Office of Pharmaceutical Science, we are currently helping a number of manufacturers develop their Comparability Protocol strategies for sterile product site changes. 

The assignment featured as an ISPE industry interview in Nov/Dec edition of Pharmaceutical Engineering and as a prioritized Commentary Article in Jan/Feb 2010 edition of PDA Journal of Pharmaceutical Science and Technology.

We are also assisting with C&Q-related aspects of a major Irish biotech expansion project and in the preparation of action plans and protocols for a client’s European, Middle East & Asia cold chain shipping process. In addition, Cliff Campbell is participating in the Knowledge Management task force of PDA’s Paradigm Change in Manufacturing Operations (PCMO) initiative.