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MedTech · Pharma · Life SciencesMaastricht · active in the Netherlands and across Europe

Who are we developing this for, who will decide on its use, and which partner do we need to move forward? Through Q22, I help companies in medtech, pharma and life sciences with those questions.

Sometimes it starts with a technology whose best application is still open. Sometimes there is already a product, and it is about a new customer, a distribution partner or an agreement. I work alongside the team, approach parties and guide the negotiations.

Ivo Schefman, founder of Q22
Ivo Schefman — founder
20+ years
commercial experience in healthcare
Partnerships
licensing, joint development and supply
Market access
experience with pricing and reimbursement
2 products
from concept to first use in patients

Expertise

How Q22 can help

Q22 supports companies from the first concept and funding through to commercialization. The customer is central at every step.

  1. Choosing an application or market

    Which customer benefits most from the technology? Together we test the need and look at who decides, who pays and what evidence is required. That helps to invest in the next development step with focus.

  2. Finding customers and partners

    Q22 identifies and approaches potential customers, development partners or distributors. In the first conversations we explore what both parties need and whether there is enough of a basis to move forward together.

  3. Making a partnership concrete

    Where there is mutual interest, Q22 helps to reach agreement on development, licensing, distribution or supply. In doing so, Q22 works with the commercial, technical, legal and regulatory colleagues who will later have to carry out the agreement.

Experience

Experience in pharma and medical devices, from concept to first use in patients

I know both sectors from practice. At companies including Johnson & Johnson, Nutricia, Allergan and DSM Biomedical, I worked in sales, market access and business development.

As co-founder of two companies, I went through the entire path with my teams: raising funding, the regulatory pathway and research in patients. In total we raised approximately €7 million in funding and grants and brought two products from concept to first use in patients.

So I know from my own experience what the consequences of a mistake along that path are.

At companies

As an entrepreneur

2018–2021

DSM Biomedical

Global Business & Commercial Development Manager

  • I handled the commercial side and the project side of medical device developments, with the largest well-known companies as well as small, promising innovations. To do so, I brought together the specialists in regulatory, engineering, quality and legal. With customers, I negotiated joint development, licensing and supply.
  • DSM Circle of Excellence 2019
  1. Since 2025 · As an entrepreneur

    Q22

    Founder

    • I work with companies on market development, customer relationships and commercial partnerships.
  2. 2024–2025 · At companies

    DynaGroup / DynaHealth

    Business Development Manager

    • I worked with healthcare partners on the practical organization of medical care for patients at home.
  3. 2018–2021 · At companies

    DSM Biomedical

    Global Business & Commercial Development Manager

    • I handled the commercial side and the project side of medical device developments, with the largest well-known companies as well as small, promising innovations. To do so, I brought together the specialists in regulatory, engineering, quality and legal. With customers, I negotiated joint development, licensing and supply.
    • DSM Circle of Excellence 2019
  4. 2017–2023 · As an entrepreneur

    Stabican

    Co-founder & Managing Director

    • As the initiator, I built up the company: from concept and funding to development partners and team. Stabican had its own analytical testing laboratory with EU GMP certification (obtained in 2022). From there, we took an active pharmaceutical ingredient into research in patients.
  5. 2015–2019 · As an entrepreneur

    Eyegle

    Co-founder & Managing Director

    • As co-founder, I went through the entire path: from concept and funding to finding development partners and building the team. With our partners, we took a DSM technology into a clinical study in humans.
  6. 2013–2015 · At companies

    Allergan

    Market Access, Pricing & Reimbursement Manager

    • For two business units, I worked on market access, pricing and reimbursement of medicines.
  7. 2008–2013 · At companies

    Nutricia Advanced Medical Nutrition

    Sales Manager

    • I led a commercial team of four for medical nutrition in hospitals, nursing homes and other care institutions, with responsibility for strategic annual plans, customer contracts and European tenders.
  8. 2004–2008 · At companies

    Johnson & Johnson Medical (Ethicon)

    Clinical Sales Specialist / Account Manager

    • I advised surgical teams on suture materials, managed hospital contracts, drew up strategic annual plans and worked on European tenders.
    • Best Sales Rep EMEA 2006
  9. 2002–2004 · At companies

    Novartis / AstraZeneca

    District Sales Manager

    • Through DOCS International, I worked in pharmaceutical sales for Novartis, Ferring and AstraZeneca.

Work experience at

Cases

Experience from practice

  1. DSM Biomedical

    Joint development, licensing and distribution

    At DSM Biomedical I expanded existing customer relationships and won new customers in areas including orthopaedics, urology and cardiovascular care. I worked with large international medtech companies and smaller companies on the development of medical devices. Together with specialists from engineering, regulatory, quality and legal, I guided development projects with a combined potential value of more than €10 million.

    With customers, I negotiated at executive level on development agreements and licence and supply agreements (LSAs). I also made agreements with distributors about the PRP system and with customers who wanted to outsource development and manufacturing to DSM (CDMO). It was in those negotiations that I learned a great deal from my colleagues. I learned from the best.

    • DSM Circle of Excellence 2019
  2. Stabican

    Co-founder and Managing Director

    I worked on building the company, its collaborations with partners and its commercial development. Stabican built a pharmaceutical platform for analysis and formulation; the organization obtained EU GMP certification in 2022.

  3. Market access and reimbursement

    Pricing, reimbursement and use in healthcare

    At Allergan I worked for two business units on pricing, reimbursement and the use of products in healthcare.

About Q22

Working with Ivo Schefman

Q22 is the independent commercial practice of Ivo Schefman.

You work with me directly. We agree on what you want to achieve, which conversations I take on and where your team stays involved. If the assignment calls for specialist knowledge, I bring in a partner from my network in consultation with you.

More about my background

Approach

From question to commercial progress

  1. Understand

    We establish who decides on a purchase or partnership and what stands in the way of the next step.

  2. Build

    We choose the customers or partners we want to approach and work out a proposal that suits them.

  3. Execute

    I make contact, hold the conversations and guide the follow-up and negotiations.

Contact

A commercial challenge in healthcare?

Would you like to explore a new market, find a development partner or bring in an experienced business developer for a period? Feel free to email me to discuss your question.

ivo@q22.eu

Maastricht, the Netherlands · LinkedIn

Get in touch