Medical Technology

avasis has been successfully serving customers in the medical technology industry for many years. Many years of experience, a number of diverse implementation projects, and the industry-specific knowledge of our team of experts allowed us to develop digital solutions for various processes in the product life cycle that meet the regulatory requirements of the medical industry.

Industry-specific solutions for digitalization

Processes in medical technology are different from the processes in other industries. Medical technology manufacturers in particular have to face a variety of different challenges: Rising health care costs, regulatory requirements, and much more. Therefore, the avasis Medical Technology team focuses on the development and implementation of digital solutions for processes and documents that meet the industry-specific requirements in terms of laws, standards, and guidelines.

We support the stakeholders of the medical technology industry in the introduction and optimization of specialized software solutions for the core issues: Product development, risk management, usability, clinical evaluation, post-market clinical follow-up, post-market surveillance, software tool validation and other ISO 13485 processes.

 

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Expertise in medical technology

Medical device companies benefit from the unique combination of our expertise in the following areas:

  • Development of medical devices and preparation of technical documentation
  • Implementation of legal requirements with focus on Europe (MDD/AIMD, MDR) and USA (21 CFR Part 820 and Part 11)
  • Efficient implementation of standards and guidelines, in particular: ISO 14971, IEC 62304 / IEC 82304, IEC 62366-1, MEDDEV 2.7/1, and MDCG guidelines
  • Detailed knowledge of ISO 13485 as well as lean implementation of required processes
  • Comprehensive knowledge of the software platform Polarion as well as its configuration and expansion
  • Agile software development and agile project management
  • Risk-based validation of software tools according to ISO 13485, ISO 80002-2 as well as 21 CFR Part 11

Together with our collaboration partners and customers we have developed inspiring solutions over the last few years: It allows you to work more efficiently and use your capacities for the development of innovative products.

avasis solutions for medical technology
Teamcenter Medical

Teamcenter Medical Device Solution

For your product development, the PLM solution “Teamcenter Medical Device Solution” supports compliance with processes and facilitates submission management, which increases efficiency significantly.

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Workflow

avaWorkflow

Management of digital templates and electronic review and approval process.

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avaRisk

avaRisk

Comprehensive solution for a risk management process according to ISO 14971 with interfaces to development, usability, and clinical evaluation.

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avaReporting

avaReporting

Comprehensive reporting functions for planning and implementation of tests as well as the representation of dependencies between information elements

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avaFMEA

avaFMEA

avaFMEA is an add-on for avaRisk and offers functionalities for the documentation of an FMEA.

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avaClinical

avaClinical

Systematic execution and updating of clinical evaluation, scientific literature reviews, state of the art description, claim management and integration with product development, risk management, and post-market surveillance

 

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avaPubmed

avaPubmed

Simplified literature search for clinical evaluations thanks to automatically executed and documented searches in PubMed and PubMed Central.

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avaPMCF

avaPMCF

Efficient updating of the clinical evaluation: Preparation of PMCF Plan and PMCF Evaluation Report as well as monitoring of PMCF activities.

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avaRegulatory

avaRegulatory

Efficient management of regulatory information & easy integration into product development

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avaUsability

avaUsability

avaUsability enables digital creation and maintenance of the usability file in Polarion and allows integration of development and risk management activities.

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avaPLMinterface

avaAdverse

Automated import of safety-related information from national authority databases, digitalized data evaluation and easy integration into clinical evaluation and risk analysis

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avaMedical StartUP! Suite

An integrated digital solution for design control documentation, regulatory requirement management and risk management activities.

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Our Mission

By developing our own digital solutions for processes in medical technology, we want to make a sustainable contribution on the following three levels:

  • Direct benefit for our customers
  • Support for the entire medical technology industry
  • Contribute to the healthcare system
avasis services

With our long-standing experience, we will gladly provide support for your digitalization project.

Your contact partner

Are you interested in digital solutions that meet the requirements of your industry? Then get in touch with our experts. We will definitely find a specialized solution for you.

Lukas Vogler
Lukas Vogler
Managing Partner & Senior Solution Architect