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/