Anne Ravnholdt Høcker joined Billev Pharma’s RA team in September. Anne has more than 20 years’ experience with writing and reviewing analytical and pharmaceutical documentation for MAAs and variations.
Anne had a strong wish to work part-time but at the same time she did not want to miss out on the challenging tasks. Now she is working four days a week and we trust that we can live up to her specialist expectations with diverse regulatory projects from our clients working in the area of small molecules and radiopharmaceuticals.
You can read more about Anne’s qualifications on our website The Billev Pharma Team.