Ivan Costa Abalo

I have over 8 years of experience in the healthcare industry, spanning both medical devices and pharmaceuticals. My career began in Buenos Aires, Argentina (where I’m from), working hands-on maintaining and repairing medical devices, an experience that gave me a strong technical foundation. Over time, I discovered a passion for education as I began training healthcare professionals on the proper use of these devices, which was very rewarding.

Later, I transitioned into data, stepping briefly outside the healthcare sector to join Mærsk Drilling, where I developed data quality indicators. This confirmed how much I enjoy the intersection of data and science, so I eventually returned to healthcare, joining Novo Nordisk as a Clinical Trial Data Manager and later moving to Zealand Pharma, where I’m currently based. This role allows me to combine stakeholder management with scientific thinking and data-driven project management.

I’m now focused on strengthening my leadership skills and growing into more strategic roles, ideally within data management, where I can continue bridging science, systems, and people.

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Frederik Bayer Frøhling

I have 5+ years of experience in the life science industry. I have been in a startup, consultancy, and a big corporation. I care deeply about creation of systems that make people thrive in their work, and enjoy supporting engineers. I want to make the best out of myself and my collegues.

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Chinmayi Bhatt

Chinmayi is a chemical engineer specializing in strategy and process development in pharma and biotech. As Process Manager at Novo Nordisk, she develops and optimizes cross-functional processes to bring drug–device combination products to market faster, ensuring scalability, robustness, and regulatory compliance. Her background spans technical sales, medical device manufacturing, and enzymatic process innovation at Novozymes, with expertise in GMP, FDA, ISO, and MDR requirements. Holding an MSc from DTU and a BEng from NTU Singapore, Chinmayi combines technical depth with strong stakeholder engagement skills, thriving in multicultural, collaborative environments.

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Carsten Schaufuss-Feddersen

Carsten is a seasoned leader with over 20 years’ experience in medical devices and drug delivery, specializing in combination products from development through filing and commercialization. He has led device teams, built organizational capabilities, and integrated combination product development into broader product strategies. With expertise spanning design controls, risk management, human factors engineering, and regulatory compliance, Carsten bridges engineering, quality, and business needs. His career includes senior roles at CSL, Alnylam Pharmaceuticals, Amgen, and NNE, where he improved quality systems, guided regulatory submissions, and supported global manufacturing and supply chain operations.

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Anna-Kathrine Fevre

I have 16+ years of industrial and private practice experience within intellectual property rights from both biotech to Pharma companies. I deliver high quality, strategic and business oriented recommendations to peers, Executives and inventors. My professional expertise spans worldwide patent litigations, due diligence, freedom to operate analysis, and leadership including mentoring of younger associates and colleagues.
I have been involved in Global Regulatory Affairs tasks including strategic considerations and input to the business on high profiled projects, building bridges between regulatory and IP departments to ensure no gaps in exclusivity rights.

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Ali Yazdanbakhsh

I have several years of experience in quality engineering within the medical device and renewable energy industries, working both in large corporations and dynamic production environments. My work has focused on ensuring product and process quality, regulatory compliance, and continuous improvement across the supply chain. I specialize in supplier quality management, nonconformance handling, and root cause investigations, and I collaborate closely with manufacturing, engineering, and quality teams to deliver high-quality solutions.

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Przemyslaw Mikulski

I have 8 years of experience within the pharmaceuticals, finance and high tech industries from large companies and in startups, – in Denmark mainly. My career has revolved around data and analytics not only from the strategic and business perspective but also from technical and engineering angles. Currently I am running boutique consultancy which specialized on building enterprise level data platforms in AWS Cloud.

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Bettina Grote

Bettina Grote is a Principal Software Process and Compliance Specialist at Oticon (Demant) with 16 years of experience in life science R&D, RA, and QA. She has expertise in design control, compliance, and documentation for medical devices, particularly in digital product R&D and SW platform processes. 

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Christian Lund Bendtsen

With 20+ years of leadership experience from Novo Nordisk A/S and the Danish Armed Forces I am truly motivated by developing others professionally and personally. My experience within the pharmaceutical business comprise manufacturing, quality, specifications, labelling and regulatory for both new product entry and lifecycle management activities.

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Sokratis Rontogiannis

Chemical engineer specialized in food technology, studied and worked in multiple countries. Working experience is in Food technology, Quality and Scaling up processes from lab scales to pilot and plant trials.

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