Ecosystem Actors

When stakes are high, generic legal advice won’t cut it. You need a lawyer who thinks like you and understands the challenges ahead.

That’s where we come in. As one of Switzerland’s first law firms dedicated entirely to the startup ecosystem, we specialize in long-term collaborations with startups focused on scaling, securing investments, and achieving successful exits, as well as with angel investors, VCs and corporate venture funds.

With years of experience in startup law and a team consisting largely of current and former entrepreneurs and angel investors, we bring a true startup mindset to everything we do. You’ll get clear advice, honest communication, and the specialized support you need.

While we’re at home in Swiss startup law, our large network of international partners and our special expertise in U.S. law allow us to facilitate expansions and cross-border transactions.

Our commitment is simple: to be the best possible lawyers for startups and investors.

We shape and steer transport development in the canton of Zurich and attach importance to ensuring that it is sustainable. To this end, we undertake strategic planning for all modes of transport and safeguard the interests of the canton vis-à-vis the federal government. The strategy and action program “DiNaMo” (Digitalization and Sustainability of Mobility in the Canton of Zurich) define the directions for future-oriented, digital, sustainable and efficient mobility development.

Swiss FinTech Association (SFTA) is the industry association that promotes the development of the Swiss FinTech ecosystem.

We shape and steer transport development in the canton of Zurich and attach importance to ensuring that it is sustainable. To this end, we undertake strategic planning for all modes of transport and safeguard the interests of the canton vis-à-vis the federal government. The strategy and action program “DiNaMo” (Digitalization and Sustainability of Mobility in the Canton of Zurich) define the directions for future-oriented, digital, sustainable and efficient mobility development.

#SwissAutonomousValley brings experts and visionary entrepreneurs together to create a one of a kind ecosystem to accelerate the development of autonomous systems in Switzerland.

With our platforms, we facilitate the exchange between technology providers, innovators and the economy with the aim of promoting and simplifying the introduction of autonomous systems in Switzerland.

As one of the leading Swiss law firms, Kellerhals Carrard offers comprehensive and interdisciplinary legal advice. We represent clients in all matters of commercial and private law – in all regions of Switzerland as well as internationally.

ISO 9001 / 13485 – Translate and adapt lean processes into simple QMS systems, support with audits, mock audits

Technical documentation for medical devices / IVD / technical

Product registration and communication with authorities

Product testing

Supply chain optimization

“Compliant medical devices for swift market access” is our credo. We support medical device manufacturers in developing medical devices in compliance with the applicable regulations from the very beginning in order to reach the market as quickly as possible.

We are specialized in active medical devices, quality management systems for medical device manufacturers and laboratories as well as software, usability, and risk management files.

As a member of various standards working groups, we are always up to date with the current state of the art and ensure that your medical devices also meet this standard.

The Winterthur Chamber of Commerce and Employers’ Association (HAW) is a business association. In the Winterthur district, HAW is the contact for exports and related formalities and information. As the regional representative of economiesuisse and the Swiss Employers’ Association, HAW represents the interests of SMEs, large companies but also startups in the Winterthur area. Together with the House of Winterthur and Technopark Winterthur, the HAW is the initiator of the Winterthur Cluster Initiative and is responsible for the Smart Machines area.

carbon connect AG is a Swiss specialist in carbon accounting, climate strategies and ESG consulting. The company supports SMEs in particular in transparently recording their emissions, identifying reduction potential and implementing specific measures in a cost-effective manner. The approach is pragmatic and entrepreneurial: instead of theoretical concepts, carbon connect provides a reliable basis for decision-making and supports companies from analysis to implementation – including financing and, where necessary, offsetting unavoidable emissions.

Effectum Medical – Your start-up to market

Effectum Medical is a young company that is breaking new ground in the areas of quality management and regulatory affairs in the medical device and in-vitro diagnostics industry.

The vision of the founders’ team is to facilitate and accelerate medical device product innovation by offering an affordable, outsourced quality management system (QMS) and legal manufacturing. Their team unites hands-on MedTech business and management experience with in-depth knowledge of regulatory affairs and quality management. The customers range from start-ups to global healthcare companies.

CETR helps European high-tech companies to access the market, industry and financial resources in China, e.g. technological application, subcontracting, supply chain optimization, regulatory compliance, commercialization and business development, as well as partnership, licensing, and investors. CETR also helps Chinese tech companies to partner and develop business in Europe.

Whether you are in the investment phase, actively developing a medical device, or seeking to position an existing device differently in the market, we provide comprehensive services for medical device development and life cycle management.

• Process-driven expertise across a wide range of medical applications (e.g. cardiovascular, orthopedics, dental, wound management, and regenerative medicine).
• Problem-solving experience in development, manufacturing, and regulatory compliance.
• Flexible support providing hands-on expertise to coverspecific project functions when resources are limited.
• Investor insights delivering due diligence and rescue strategies to protect your investments.

Quality Management

A robust Quality Management System (QMS) is the foundation of regulatory compliance and market readiness. We help medical device companies implement and customize eQMS solutions aligned with ISO 13485, FDA 21 CFR 820, MDR/IVDR, and MDSAP. Our approach transforms quality from a compliance obligation into a strategic advantage.

• eQMS implementation
• Auditing

Regulatory & Clinical Affairs

We guide our customers in defining regulatory and development strategies that accelerate time-to-market, ensure compliance and reduce costs. By combining global submission expertise, product risk classification, and robust clinical evidence, we help turn complex regulatory pathways into a business strategic leverage.

• Smart strategy for faster, compliant market access
• Submissions
• Documentation
• Clinical Evidence
• Authority Interactions

Product Development

From concept to commercialization, compliance and patient safety must be embedded in every stage of product development. We integrate biocompatibility (ISO 10993), usability engineering (IEC 62366), risk management (ISO 14971) into your processes. This ensures safe, effective, and user-centered devices that meet regulatory requirements and accelerate time-to-market.

• Project Management
• Biocompatibility
• Risk Management
• Usability & Human Factors Engineering

Due Diligence for Investors

Investing in medical devices carries regulatory, clinical, and technical risks. Our due diligence assessments provide a reality check of QMS maturity, regulatory compliance, product readiness, and risk exposure, empowering investors with the data-driven insights needed to make confident investment decisions and reduce market entry uncertainty.

• Regulatory Review
• Product Readiness
• Gap Analysis

Due Diligence for Investors

Investing in medical devices carries regulatory, clinical, and technical risks. Our due diligence assessments provide a reality check of QMS maturity, regulatory compliance, product readiness, and risk exposure, empowering investors with the data-driven insights needed to make confident investment decisions and reduce market entry uncertainty.

• Representation
• Verification
• Swissmedic Liason
• Monitoring

At Congenius, we offer tailored medical technology consultancy services in the fields of Quality, Regulatory, eHealth, Operations and Clinical. Our goal is to enable the smartest route to enhanced medical solutions.

Together with our customers, we stimulate informed ideas, create lasting solutions, and inspire positive change. We provide tailored expertise and leadership to global firms, established SMEs, and aspiring start-ups in the medical device, in vitro diagnostics, and pharmaceutical industry. By reassuring our customers through knowledge and experience we form trusted partnerships that facilitate the successful registration and delivery of medical devices.

If you`re a customer looking for support with your next challenge, please feel free to get in touch via our website, or by sending our CEO Bastian Perroset a message – we look forward to speaking with you.

As our customer base and service portfolio continue to develop and grow, we also welcome applications from experienced candidates looking to join our dynamic organisation. If you enjoy working with a diverse range of people across a broad range of projects and are passionate about making a positive contribution to the medical technology industry, then a role as a Congenius Consultant could be your next rewarding career step. Take a look at our job postings for our available roles.

inmedis is your partner if you are looking for competent support in quality management and regulatory affairs in medical technology. Our experienced experts advise and support you with certifications, personnel bottlenecks and many other QM/RA issues. To help you reach your goals faster.

Swiss Association for Environmental Technology (SAET) is intensively committed to the development of a safe and future-oriented environment, energy, waste and water management. It brings together the expertise of the movers and shakers: manufacturers, suppliers, operators and planners in environmental technology. As the Swiss Association for Environmental Technology, SAET works independently and is a dialog-strong discussion platform with national and international appeal for experts from business, research and industry.

Telling your innovation story using your data and your processes. We make your organization data driven by taking any use case from idea to finished product / service in 12 weeks. Across the following areas of domain expertise we have helped global corporates, small & medium enterprises as well as scale-ups:

• Regulatory Improvement & Efficiency
• Sustainability Transformations
• Data Management & Data Architecture
• Digital Upskilling
• Smart Real Estate, Smart Supply Chain & Smart Logistics

Autonomous technology will fundamentally change mobility as we know it today. The mission of the Swiss Association for Autonomous Mobility (SAAM) is to enable the introduction of new technologies and offerings in Switzerland for a common good.

Into the future with safety As part of the SVTI Group, Swiss Safety Center AG is committed to providing specific services, products and qualifications in the field of safety and quality. Swiss Safety Center AG offers solutions for all industries with specific services, products and qualifications in the field of safety and quality. This includes inspections, tests, certifications, assessments, expert opinions as well as training and further training in the areas of risk management, occupational safety, fire protection, material safety and many other specialist areas of technical safety and certifications in all sectors in accordance with the well-known management system standards (ISO 9001, ISO 14001, ISO 45001, ISO/IEC 27001 etc.).

Konsento – The smart solution for corporate actions in Swiss AGs

Konsento digitizes and simplifies central corporate actions of Swiss stock corporations – from the share register to general meetings and capital increases. The platform creates efficiency, transparency and legal certainty in the management of equity structures.

Our core functions

• Digital share register: Existing registers can be imported, supplemented and kept up to date. Shareholders can maintain their data themselves, transactions are documented in a traceable manner and the legality of previous entries and transfers can be easily checked.
• Digital general meetings: From invitations and voting to the certification of resolutions and the automatic creation of minutes – everything is legally compliant, efficient and, depending on requirements, physical, purely online or hybrid.
• Efficient board meetings: Digital agendas, voting and automatic minutes facilitate the work of the Board of Directors.
• Digital capital increases: From resolution to entry in the commercial register – fast, compliant and cost-efficient. Including access to notaries available at short notice.

The advantages at a glance

• Less effort: Automated processes save time and resources.
• More legal certainty: Legally sound and in line with current legislation.
• Clear transparency: strengthens trust among shareholders and the Board of Directors.

More than 350 Swiss stock corporations already rely on Konsento to make their corporate governance digital and future-proof. Whether you’re a startup or an established SME – with Konsento you can manage your equity efficiently, intuitively and in compliance with the law.

For more than 25 years, DHC Dr. Herterich & Consultants Group, with its two main locations in Saarbrücken (D) and Zurich (CH), has specialized in Software Validation (CSV) in the life sciences industry. Working in the regulated environment, we have become the specialist for Quality Management and GxP Compliance . Our field-tested and preconfigured SAP solutions for quality control and quality assurance are therefore no longer used only in the Pharmaceutical industry and Medical technology for use, but also in other industries.

The know-how of the excellently trained DHC Consultants is characterized by a combination of process and industry knowledge in conjunction with excellent IT skills, taking into account compliance requirements.

This leads to a significant acceleration and quality improvement in the projects. The conception and implementation of our projects is process-oriented in order to be able to guarantee a maximum of economic benefit.

In order to meet the high demands on core processes in the life sciences (e.g. in quality and IT management as well as in the logistics of pharmaceutical companies) and the supporting IT systems, we developed our own innovative solution approaches, best practices, methods and services right from the start.

www.dhc-ag.ch

The Zurich Chamber of Commerce ZHK represents the interests of its approximately 1,100 members and networks them with each other and with external partners. The ZHK builds bridges between companies, politics, and society and advocates liberal and market-based framework conditions for companies. ZHK also offers customized services in the areas of export and law.