() Research and development and regulatory affairs | Norbrook

Research and Development  and Regulatory Affairs

Using leading edge technology, our scientific teams create the products of the future to enhance the health and well being of animals all over the world. Our state-of-the-art laboratories and latest technology ensures our scientific teams are equipped to create an exciting and robust innovation pipeline.  

Help us solve complex and challenging work

Our Research & Development department plan and co-ordinate the development of novel and differentiated generic products from formulation through to clinical trials. This is completed to GLP (Good Laboratory Practice) and GMP (Good Manufacturing Practice) standards. This department also provides support to our Regulatory Affairs team who are then responsible for steering the new product application through to registration. Global data requirements may differ depending on the geographical location and diverse regional legislation.

Our Regulatory Affairs department are therefore highly skilled in understanding the nuances of regulatory requirements and negotiating with agencies in order to progress variations to existing products as well as gaining approvals for new products.

Our Technical Validations Team are responsible for providing documented evidence that all our processes, procedures, facilities and equipment perform compliantly and consistently. Each year this team complete in excess of 600 projects. Their work not only supports routine manufacture of existing products but also ensures the optimisation of processes etc. for new products.

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