About BioQC
BioQC is a global knowledge platform for scientists, researchers and innovators involved in the development and manufacturing of biopharmaceuticals and biologicals, helping to bring better biopharma products to life.
The BioQC Platform
We help translate complex technical and regulatory topics into information that is easier to understand, apply, and share. Our goal is to support the people behind biopharma innovation by providing educational resources that are relevant, credible, and useful in real development settings.
BioQC delivers in-depth, expert-driven content and facilitates meaningful discussions on the challenges and innovations in CMC (Chemistry, Manufacturing, and Control) strategies, as well as the regulatory considerations that shape drug development.
We provide expert insights through webinars, expert forums, learning hubs, educational materials (including articles, application notes, eBooks, videos, etc.), and a vibrant user community.
Why BioQC Started
Biopharma drug development advances rapidly, yet the information required for CMC and regulatory planning is often dispersed, complex, highly technical, or difficult to access.
BioQC assists at every phase of drug development, from First-in-Human (FIH) trials to market approval, by providing expertise in clinical development and regulatory review. This approach enhances decision-making, encourages collaboration, and strengthens confidence throughout the process.
Equally important is QC; quality must be controlled constantly and consistently across all stages of biopharma drug development. This ensures more robust processes, shorter development timelines, and safer, higher-quality production of medicines for patients worldwide.
BioQC’s Approach
Topics
Our topics focus on CMC strategy and development, regulatory education and interpretation, and practical insights for biopharma scientists and researchers.
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Quality Experts
BioQC partners with leading experts shaping the future of biopharma, uniting specialists from key disciplines involved in the biologics lifecycle.

Dr. Christof Finkler
F. Hoffmann-La Roche AG

Dr. Pierre Lebrun
Cencora – PharmaLex

Dr. Anne Ries
Boehringer Ingelheim

Dr. Eric Rozet
GSK

Dr. Cyrille Chéry
UCB

Prof. Sandra Furlanetto
University of Florence

Dr. Patanachai "Kong" Limpikirati
Chulalongkorn University

Dr. Lars Geurink
Batavia Biosciences

Dr. Simona Cianetti
GSK

Dr. Joachim Ermer
Ermer Quality Consulting

Dr. Bingchuan Wei, MBA
Genentech

Dr. Francisca Galindo Garre
Johnson & Johnson Innovative Medicine

Jon Walker
LabWare North America

Dr. Ejvind Mørtz
Alphalyse

Dr. Adam Sutton
Merck

Dr. Lu Huixin (Lulu)
Health Canada

Melanie Clark
LabWare North America

Dr. Jennifer Rea
Genentech

Dr. Timothy Blanc
Eli Lilly and Company (retired)

Ramon de Groot
Limes Lab Support

Paul Schrevel
Solution Too

Dr. Carmilia Jiménez Ramírez
Miliar Biopharma Solutions

Dr. Joseph Glajch
JLG AP Consulting

Dr. Michael Dong
MWD Consulting

Gloria Slomczynski, MBA
Laboratory Informatics and Management Consultant

Dr. Jean-François Dierick
GSK

Giovanni Vitali, MSc
GSK

Dr. Thomas Kofoed
Alphalyse

Asa Curry, MSc
Spur Therapeutics

Dr. Somar Khalil
GSK

Derrick Zhang, M.Sc
US Pharmacopeia

Dr. Eef Dirksen
Byondis

Dr. Anette Draborg
Alphalyse

Dr. Søren Skov Jensen
Hemab Therapeutics

Assoc. Prof. Dr. Marieke Klijn
Delft University of Technology

Dr. Lorenz Liesum
Roche

Dr. Christof Finkler
F. Hoffmann-La Roche AG

Dr. Pierre Lebrun
Cencora – PharmaLex

Dr. Anne Ries
Boehringer Ingelheim

Dr. Eric Rozet
GSK

Dr. Cyrille Chéry
UCB

Prof. Sandra Furlanetto
University of Florence

Dr. Patanachai "Kong" Limpikirati
Chulalongkorn University

Dr. Lars Geurink
Batavia Biosciences

Dr. Simona Cianetti
GSK

Dr. Joachim Ermer
Ermer Quality Consulting

Dr. Bingchuan Wei, MBA
Genentech

Dr. Francisca Galindo Garre
Johnson & Johnson Innovative Medicine

Jon Walker
LabWare North America

Dr. Ejvind Mørtz
Alphalyse

Dr. Adam Sutton
Merck

Dr. Lu Huixin (Lulu)
Health Canada

Melanie Clark
LabWare North America

Dr. Jennifer Rea
Genentech

Dr. Timothy Blanc
Eli Lilly and Company (retired)

Ramon de Groot
Limes Lab Support

Paul Schrevel
Solution Too

Dr. Carmilia Jiménez Ramírez
Miliar Biopharma Solutions

Dr. Joseph Glajch
JLG AP Consulting

Dr. Michael Dong
MWD Consulting

Gloria Slomczynski, MBA
Laboratory Informatics and Management Consultant

Dr. Jean-François Dierick
GSK

Giovanni Vitali, MSc
GSK

Dr. Thomas Kofoed
Alphalyse

Asa Curry, MSc
Spur Therapeutics

Dr. Somar Khalil
GSK

Derrick Zhang, M.Sc
US Pharmacopeia

Dr. Eef Dirksen
Byondis

Dr. Anette Draborg
Alphalyse

Dr. Søren Skov Jensen
Hemab Therapeutics

Assoc. Prof. Dr. Marieke Klijn
Delft University of Technology

Dr. Lorenz Liesum
Roche
Leading Organisations
Our quality experts work at leading global organisations or consultancies, understanding real-world operational needs and demanding technical & compliance standards.
Knowledge sharing is our solution, quality is our promise
BioQC is focused on making specialised knowledge more approachable without losing scientific depth. Our digital-only platform is designed to be more than a source of information; it is a space where technical expertise, regulatory perspective, and educational value come together in service of innovation.
Ideal for scientists seeking trusted educational content that combines clarity, relevance, and technical insight. It is particularly beneficial for scientists, researchers, or industry innovators who cannot attend in-person conferences and events.
Our scientific directors, Prof. Dr Cari Sänger-van de Griend and Dr Ewoud van Tricht, bring extensive experience from academia and industry, including AstraZeneca, Solvay, Abbott, Janssen, and Sanofi. They help tailor and moderate expert-led online webinars and active panel discussions.
Our Values
- Clarity.
- Relevance.
- Scientific rigour.
- Knowledge sharing.
- Accessibility.
- Progress through learning.
Join Us
If you seek educational insights on CMC strategy and regulation, we are here to help you learn, connect, and progress with confidence.
We serve researchers, scientists, innovators, and other professionals involved in biopharmaceutical drug development. Whether you are early in the development process or working through more advanced technical and regulatory questions, BioQC is here to help make the path clearer.
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Sponsorship and advertising options are available for lead generation, sharing scientific insights, thought leadership, product launches and enhancing branding and awareness.
Let’s Connect
If you’re seeking a reliable partner that values quality and trust, we would be pleased to hear from you. Contact us to discuss how BioQC can collaborate with you or your organisation.
Our team focuses on clear communication, careful execution, and a high standard of work, enabling collaborators and clients to trust both the process and the outcome.

Extraordinary Prof. Dr. Cari Sänger-van de Griend
Scientific Director
Prof. Dr. Cari Sänger–van de Griend is a founder and scientific consultant at Kantisto and an associate professor at Uppsala Universitet in Sweden. Cari holds an MSc in BioPharmaceutical Sciences from Universiteit Leiden and a PhD and Habilitation in Analytical Pharmaceutical Chemistry from Uppsala Universitet. She has previously worked with Astra Pain Control, AstraZeneca, Solvay Pharmaceuticals, and Abbott Healthcare Products, focusing on small molecules, therapeutic proteins, vaccines, and nucleotides. In her daily role, Cari supports industry, institutes, and academia in the realm of (bio)pharmaceutical analytical chemistry and Analytical Quality by Design (AQbD). She is dedicated to sharing knowledge and fostering scientifically sound decisions with the patient in mind.

Dr. Ewoud van Tricht
Scientific Director
Dr. Ewoud van Tricht has over 18 years of experience in the (bio)pharmaceutical industry. He has worked on small molecules, antibodies, proteins, viruses, and cell therapies at companies such as Abbott Healthcare Products, Janssen Vaccines, and Sanofi Cell Therapy. Alongside his full-time career, he completed a Bachelor’s, Master’s, and PhD in Analytical Chemistry. Ewoud specialises in Analytical Quality by Design (AQbD), having developed and implemented strategies to enhance pharmaceutical methods. He is passionate about optimising processes, coaching teams, and driving innovation through AQbD, Agile, and Lean methodologies, always striving for efficient and impactful results.
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