JensonR+ was formed in 2011, through a joint venture with the regulatory consultancy, Dr Regenold GmbH.
Our clients range from small innovators and entrepreneurs, through to Blue Chip corporations, and come from the human and veterinary pharmaceutical, cosmetics, foods, devices, herbals and legal industries.
Our specialist team is experienced in regulatory affairs, product development, quality assurance, drug safety, medical information, copy approval, project management, training and market access.
We can provide support at all levels, from strategy through to administration, which allows us to tailor our services to meet your specific needs as your company moves from innovation and development to the market place.
We use forensics, knowledge and experience to challenge your thinking and to guide you where you need it. We make sure nothing is missed so that your project is fit for purpose and delivered ‘on time’.
We achieve all of this by calling upon our wide range of in-house technical experts. Our team is based both in the UK and Europe with our office in Dublin and has successfully developed products from concept through commercialisation.
If you like what we do, we will appoint a skilled and experienced project manager who will become an extension of your own team. They will support you and act on your behalf. We work with, and coordinate, a series of preferred suppliers to provide outsourcing solutions, from API suppliers to manufacturers, CROs and laboratories.