About Forcentis
Your Partner in Compliant Medical Devices Manufacturing
We deliver the security required to fix volatile situations and transform complex regulatory requirements into a compliant day-to-day production situation.

Our Role: Expert Advocacy for Operational Certainty

Forcentis operates at the critical intersection of MedTech regulation, engineering, and manufacturing. We are founded on the principle that compliance should be an accelerator, not an obstacle. Our deep interdisciplinary understanding of the entire supply chain, from equipment manufacturer to legal manufacturer, allows us to provide tailored solutions and act as your trusted advocate in every project phase.

Facts & Figures

Expertise You Can Measure

Our history is defined by results, not just promises. These metrics quantify the depth of our specialization and our unwavering commitment to client success and sustained reliability across the MedTech supply chain.
14

of specialized MedTech Experience

500

Process and Equipment Risk Assessments Conducted

200

Successful Projects Completed

90

Client Repeat Engagement Rate

55

Unique Medical Device & IVD Types

Values

Our Guiding Principles

Our mission and vision reflect our commitment to excellence, technological relevance, and support for our clients in a highly challenging regulatory field. They define the impact we strive to have on project outcomes and the global supply chain.

Our Mission

Our mission is to bridge the gap between complex regulatory requirements and their practical implementation within the manufacturing environment of medical devices and IVD .

We provide customized consulting services rooted in a deep understanding of our customers’ individual situations. By anticipating challenges, accelerating decision-making, and delivering reliable solutions, we empower our clients to achieve compliance and success.

Our Vision

Our vision is to be the most trusted partner for the manufacturing of medical devices and IVD.

We aim to be the premier provider of expert guidance in the MedTech manufacturing ecosystem. By delivering unprecedented and reliable services, we enable innovative and compliant solutions, significantly improve risk control, and accelerate stability throughout the global supply chain.

Our Team

Experts and Advocates

Our success is driven by our people. Every member of the Forcentis team combines deep technical competence and regulatory competence with empathy, ensuring you receive the highest level of expertise, personal commitment, and hands-on support for your most critical projects.

Michael Roth

CEO

+41 79 372 98 90
michael.roth@forcentis.com
Contact

Felix Freudiger

Senior Consultant

+41 78 230 77 27
felix.freudiger@forcentis.com
Contact

Carolina Salenius

Senior Consultant

+41 78 262 02 36
carolina.salenius@forcentis.com
Contact
Our Journey

A History of Specialization

Since 2012, we have been shaping the compliance field for the manufacturing of medical devices and IVD, marked by deep collaboration and the continuous expansion of our specialized services.
  • 2012
    Forcentis was founded on June 2, 2012, by Dr. Karl Weis. Immediately began collaboration with leading Equipment Manufacturers, Contract Manufacturers, and Legal Manufacturers.
  • 2013
    Initial deployment of our Proprietary FMEA Tool in client projects, enhancing risk assessment efficiency.
  • 2017
    Successfully executed our first project in North America, marking the start of international expansion.
  • 2018
    Completed our first project for an IVD Instrument (in vitro diagnostics).
  • 2019
    Secured our first project involving Single-Use Systems (SUS) for Biopharma Manufacturing, diversifying our niche expertise.
  • 2021
    Forcentis AG was acquired by Michael Roth.
  • 2022
    Headquarters relocated to the current facility in Horw.
  • 2022
    Forcentis AG secured a Personnel Leasing License for national and international personnel secondment.
  • 2023
    Successfully executed our first project in Latin America.
  • 2025
    Established a partnership with InteQRA GmbH to expand services to cover the regulatory approval (Zulassung) side of Medical Devices.
  • 2026
    Re-branding of Forcentis
    Expert Perspectives

    Regulatory Insights & Knowledge

    Stay up-to-date with the regulatory landscape and gain practical knowledge from our specialists on critical topics spanning validation, implementation strategy, and compliance.
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