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Regulatory affairs advice for new products

We work with clinical research organisations helping to take products from the early drug development stage through to marketing authorisation. Our regulatory affairs specialists are experienced guiding and transferring their knowledge to your team ensuring your product progresses to the next step.   

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Regulatory Affairs Project Manager

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We always provide a highly individualised service and are proud of being recognised for going that extra mile to support our clients.


About Lisa

Regulatory Affairs Project Manager

Lisa’s experience covers the product lifecycle, from early development to post marketing support. Working with drug development companies she has provided clinical regulatory support which has involved IMPD and IB authoring as well as preparing and submitting CTAs.

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