Regulatory Life Cycle
We help medical device companies in meeting the new, comprehensive requirements and compliance expectations during the entire lifecycle of their products all around the world.
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Regulatory Lifecycle for Medical Devices
Medical devices are regulated around the world. But as medical device definitions vary in different parts of the world as well as classifications, activities required may vary. Therefore it is beneficial to plan your target markets in the regulatory plan(s) to be able to plan activities better. This allows smooth global registrations and reduced time to market. So if you are planning a product for the US market and after that for the EU and Australia, it is worth qualifying and classifying your product in all of these planned target markets. This is applicable especially if it looks like the device is not a medical device in your initial target market, for example in the US, but it might be somewhere else. It may affect heavily on the development activities. Labquality has experience in various markets.
Design
There are several common aspects of technical documentation around the world. The most simplified pattern is:
The whole design process must be covered by the design and development (or design control) process of the manufacturing company. Their requirements and risks are identified in the first place to understand what user wants, and what are the requirements and related risks. This is similar everywhere. Although requirements and risks must include all the required aspects and the team thinking requirements and risks must have someone familiar with requirement and risk management processes, Labquality has those experts to support you.
After defining phase, the product is designed, tested and transferred to production. Each of these steps contains a significant amount of documentation ie evidence, including specifications, test plans and reports, work instructions and device technical documentation. A significant part of the evidence for compliance is the clinical evidence. Especially EU regulations have increased such requirements, thus clinical evidence must be solid. This starts with clinical evaluation which often needs to be supported by pre-market clinical investigation. Labquality can operate as your trusted CRO.
Regulatory lifecycle
After CE marking, FDA clearance or approval or other local sales approval, the manufacturer must maintain technical documentation, and inform changes to authorities where mandatory. Labquality has experts to monitor regulatory landscape changes and perform the activities needed to keep medical devices in the desired markets. Most of the markets require active post-market surveillance (depending on the risk level) and active reporting to authorities. Labquality provides also post-market surveillance as a service (PMSaaS). So keeping product on multiple markets simultaneously require some work and an organised mindset.
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Labquality
How can we help?
Labquality can support you in
planning regulatory pathways
documenting target market requirements to regulatory plan(s)
performing qualification and classification for each target market
supporting in design and development processes
supporting in all technical documentation
performing clinical evaluation planning and reporting
clinical investigation planning, data management, execution and reporting
Explore our services

Electrical Safety IEC 60601
IEC 60601-1 is the basic safety standard for medical electrical devices and systems.
Biological Safety ISO 10993
We provide medical device manufacturers help with setting up a biological safety evaluation process and preparing biological evaluation documentation.
IVD Performance Evaluation
Labquality helps manufacturers comply with the clinical evidence requirements of the IVD Regulation.
Risk Management ISO 14971
Labquality provides medical device manufacturers help in setting up and implementing a risk management system and preparing risk management documentation.
Regulatory plan
Labquality can help medical device manufacturers in creating a regulatory plan.
Qualification and classification of medical devices
Our team’s versatile experience and the available tools help in bringing clarity to the challenging cases.
IVDR compliance for in-house developed tests
Laboratories developing IVDs in-house must maintain Technical Documentation and Quality Management Systems to comply with the IVDR and the national law.
Medical software
Labquality also provides comprehensive support for medical software lifecycle.