Karin Bryder
CEO
PhD in medical science, long experience in pharmaceutical development, medical technology products and patent strategies.
Responsible for the company’s ongoing operations and to implement the Board’s strategic decisions. “Takes the ball” and runs with it for a while before passing it on.
Kerstin Wäborg
BD Sweden
Responsible for contacts with distributors and in connection with public procurements in Sweden.
Previous experiences include Nordic Sales Manager, Enzymatica AB, Regional Manager/Consultant, MSD, Abbott, Alcon, District Manager, KAM, Product Specialist, Glaxo, Sales Manager, Yamanochi Pharma, Product Manager, Nordisk Insulin/Novo Nordisk.
Carina Lindqvist
BD Europe
Responsible for contacts with distributors in Europe.
Previous experiences include CEO, Ellen AB with subsidiaries in China, CEO, Sweden Recycling with responsibility for the Nordic region, Sales and Marketing Manager, Ferrosan AB/Pfizer, European Product Manager, Dentsply.
Karianne Ellekrans
CMO
Responsible for marketing and contacts with the consumer market as well as the company’s entire visual expression.
Previous experiences include Marketing & Brand Manager, Attivia/Standard Innovation Corporation, Founder/Business Developer, Loop Health AS (formed in 2013 and acquired in 2015), Founder/CEO, Laid AS (formed in 2009, acquired in 2015).
Ola Skanung
CFO
MSc in Business and Economics with specialisation in entrepreneurship with further studies in Change Management and auditing.
Many years of experience as CFO in listed companies, extensive experience from working with fast-growing, innovative companies.
Helene Dahlberg
SCM
Systems Development Engineer with many years of experience in request for information and follow-up in product development and purchasing.
Responsible for processes within logistics and purchases. Follows up on quality, delivery time and costs. Handles the implementation of the company’s internal business system, interaction with external parties and IT security.
Ulrika Andersson
QA & RA
Chemical engineer with solid additional training and experience in, among other things, quality and environmental management systems.
Responsible for and manages the company’s quality management system and regulatory compliance. Handles regulatory issues for markets in and outside of Europe.
Elisabeth Sthengel
DDM/CDM
MSc – Biotechnology with long experience in the development of medical technology devices and clinical studies.
Responsible for new products in the portfolio and their development within the framework of the applicable regulations. Responsible for sponsorship in clinical and aftermarket studies.
