Unlike any other vendors in the arena of providing Informatics solutions to the Pharmaceutical industry, Novatek provides customers with a truly scalable approach to implementing systems in a timescale and sequence which meets their priority needs, rather than the system requirements of the software.

Customers can choose to deploy a fully functional Stability or Environmental Monitoring system in the initial instance, and then phase in additional application modules as requirements and priorities dictate.

 

Many customers choose to implement the Novatek modules to augment their existing LIMS which have limited capabilities to perform Stability Management or Environmental Monitoring, we understand what is required at every step of the manufacturing process and leverage that knowledge to improve your quality processes. Your project will be up and running with a minimum of effort and downtime.

The resulting solutions comprise a state of the art, integrated informatics solution, addressing all areas of our customers business, and are fully compliant with the regulatory needs of FDA 21CFR part 11.

As the Novatek portfolio is designed not only with this integration in mind, but also with the rigours of regulatory requirements, the implementation and validation overhead is significantly reduced by utilizing the Novatek validation package, which together with implementation services provided by Novatek, ensure that the installed system is fully validated to the latest standards.

Novatek’s experience in this arena provide our customers the opportunity to deploy a cost effective Pharmaceutical solution, with minimal interruption to normal business processes, and to enjoy the return on investment more quickly than is achievable by traditional LIMS systems.

Novatek are uniquely well placed to deliver on this promise due to the innovative way in which the applications are designed and deployed. The applications are stand-alone in their own right, and can be brought into productive operation in discrete phases.