Look for our booth #18, right next to our partner Medfiles at booth #17! Together we form a strong Nordic and Baltic alliance to support in a stronger scale pharma, medical device, IVD and veterinary companies with a wide range of regulatory support including translations, maintenance, regulatory submissions, regulatory expertise support, strategic advice, including pharmacovigilance, and also within clinical operations related tasks.
This conference is bringing together the pharmaceutical, medical device and veterinary communities for the first-choice key event in the European regulatory affairs for anyone working as, or alongside, regulatory professionals.
Don’t miss meeting our regulatory expert team:
Link Medical Research:
Grethe Berven
Director Regulatory and Safety – Norway
Grethe.Berven [at] linkmedical.eu
LinkedIn
Anne Kræmmer
Director Regulatory and Safety – Denmark
Anne.Kraemmer[@]linkmedical.eu
LinkedIn
Marianne Jonsson
Director Regulatory & Safety – Sweden
Marianne.Jonsson[@]linkmedical.eu
LinkedIn
Marianne Holst
Executive VP Regulatory
Marianne.Holst[@]linkmedical.eu
LinkedIn
Arne Saupstad
BD Managament
Arne.Saupstad[@]linkmedical.eu
LinkedIn
Medfiles:
AnnaAlonen
Manager, Regulatory Affairs
anna.alonen@medfiles.eu
LinkedIn
MaijaJokela
Manager, Regulatory Affairs
maija.jokela@medfiles.eu
LinkedIn
Tuuli Marvola
Manager, Business Development
tuuli.marvola@medfiles.eu
Päivi Turta
Manager, Regulatory Affairs (MD/ IVD)
paivi.turta@medfiles.eu
LinkedIn
You are very welcome to meet us at booths #17 and 18 for information and discussions about our services and how we may support you in your product development and resourcing needs.
We are looking forward seeing you.
