There is simply no ISO standard for inefficiency.
We don’t just talk about efficiency, we embody it.
As an owner-managed company for more than 25 years, we have stayed true to our principles and continuously strive for efficiency and effectiveness, including in our own operations.Why grow into a large organization? 99% of all compliance tasks are best solved by a small, dedicated team.
Our Flexibility and Efficiency
Our drive is to meet our clients’ needs through tailored and transparent solutions.
Effectiveness, traceability, and efficiency are our top priorities. Our employees are highly trained to achieve these goals and maintain direct, short communication channels, ensuring the highest quality at all times.
We are certified according to ISO 13485:2016 (German/English) and advise companies in the medical technology, biotechnology, and pharmaceutical industries on the implementation and streamlining of MDD/MDR/IVDR approval and GMP projects. We apply the same standards to our own work. This means we always recommend the fastest and safest route to the project objective and only charge for the actual effort that can be clearly demonstrated.
Thanks to our agile team, we can offer clients the flexibility to respond quickly with our qualified consultants and specialists, even under time pressure. No time is wasted, as our team members are perfectly attuned to each other through many joint projects. Our clients benefit from this flexibility far beyond traditional holiday or sick leave coverage.
Our Clients
Among our clients are small businesses as well as medium-sized companies and global players. Project volumes therefore range from €1,000 to €3,000,000. Due to strict confidentiality agreements with most of our clients, we are only permitted to publish a small selection here.
Our History:
1999
Company founded by Jürgen Grünewald in Heppenheim, with a focus on “lean” documentation in the pharmaceutical industry to ensure compliance with regulatory requirements in qualification and validation.
2001
Systematic establishment of a risk-based approach to validations in the pharmaceutical industry
2004-2005
Expansion of the service portfolio to meet regulatory and normative requirements in the medical device industry
2007
First risk-based approach applied to the relocation of regulated production areas during ongoing operations
2012
Continuous growth and relocation within Heppenheim
2015
Expansion of the service portfolio to include normative and regulatory requirements in biotechnology
2018
Acquisition by Szilárd Varga and renaming of the company to Grünewald GmbH & Co. KG
2019
Change of legal form to GmbH: The now well-known name Grünewald GmbH is established
2020
Grünewald is certified according to the medical device standard DIN EN ISO 13485
2021
New construction and relocation to Bensheim into a new office building with capacity for up to 80 employees
2023
Nearly 40 experts handle projects for clients, and Grünewald is a preferred supplier for renowned companies and international corporations.
Meet some of the Grünewald experts
Our Expertise and Consulting Competence
Thanks to the solid academic background of our team members, we are able to fully understand your challenges and develop smart solutions.
Our employees are biologists, chemists, process engineers, and engineers working across different industries, locations, and interdisciplinary teams. Strong social skills and deep expertise are the key success factors of our work.
We are happy to share our experience with our clients and continue to grow through the exchange with their specialists in the numerous projects we support.
We look forward to your call!
For (potential) clients:
Dipl.-Ing.
Szilárd Varga
Managing Director,
Head of Customer Care & Sales
For all other inquiries and topics:
Andrea Wladarz
Financial Accountant / Assistant