Our specialist team here at JensonR+ is experienced in regulatory affairs, product development, quality assurance, drug safety, medical information, copy approval, project management, training and market access.

Here we share insights into our ways of thinking in this changing landscape. Any questions please talk to us, we are happy to start the conversation.


Jenson R+ Limited can assist you with compiling the necessary data and making variations to maintain the lifecycle of your product, we can help through an end to end submission or by providing advice and guidance to help you keep your medicine complaint and on the market.

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