INSAKATO Consulting

INSAKATO is a Nordic family-owned consultancy offering services primarily within the medical device sector.

The company has offices in Malmö, Stockholm, and Sälen and also operates from an office in Copenhagen (DK).

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Our Team

Torbjörn Lindberg

Born 1964, PhD in Materials Science [KTH, Sweden]. Torbjörn possesses extensive knowledge and experience in materials and surface modifications, predominantly within the medical devices businesses. Torbjörn is also an expert in the ISO10993-1 standards and its subclauses, being part of the expert group S-258 at Dansk Standard.

Torbjörn is the head of INSAKATO and oversees all operations.

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Vincent Lindberg

Born 1999, MSc at [CBS, Copenhagen] and current student in Applied Mathematics [LTH, Sweden]. Vincent provides extensive knowledge of statistical analysis predominantly through multivariate analysis, employing Python and Excel.

Beyond this, he applies his economics skills to run the financial division of INSAKATO.

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Ludvig Lindberg

Born 1999. PhD Candidate in Computational Fluid Mechanics [Lund University, Sweden].
Ludvig holds a Master of Science in Mechanical Engineering [LTH, Sweden], with a specialization in Computational Fluid Dynamics (CFD). He has expertise in mathematical modeling, numerical analysis, and reactive transport phenomena in porous media.

He applies his skills in aiding operations at INSAKATO where relevant.

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Cay Lindberg

Born in 2002, a student in Medical Engineering [KTH, Sweden]. Cay is currently pursuing a Master’s degree in medical sensors and data management, but possesses a holistic view of the industry and is skilled in several aspects of the sector.

She is also proficient in software development, web design, and all Microsoft software, and is therefore responsible for IT at INSAKATO.

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INSAKATO possesses an extended network of specialist covering electrical, software, managerial and project management competences which may be consulted upon requirements from any customer. Vision

Our Core Competences

EN 60601
MDR and IVD
ISO 14971
ISO13485
ISO10993
21 CFR 820
Process Validation according to GHTF/SG3/N99-10:2004
Design Qualification including Method Development; verification and validation.
Reprocessing of Medical Devices
Surface Modifications applied by different chemistries and radiation supported methods.
Supplier assessments of medical device supply chain in an international environment.

We offer both long- and short-term contracts.

Please contact us for further information.