and our team working with preparation and review of analytical and pharmaceutical documentation is growing.

In May Lone Pallesen, B.Sc. Ing. in chemistry joined our regulatory team. Lone holds a Diploma in Regulatory Affairs from Medicademy and has more than 20 years’ experience within this field. She is specialised in quality/CMC requirements and in writing and review of module 3 documentation.

You can read more about Lone’s qualifications here: http://billevpharma.dk/about-2/staff/

We experience increasing demand for our regulatory services

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