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EMSIDO provides technical services related to design and development, Concept feasibility study, FEA, testing, and regulatory submission of a range of automation devices. We can work on a project basis, or we can engage in short or long terms team contracts to help you achieve your objectives. Contact us today by booking your desired service shown below.
Our consultants are subject matter experts, combining FDA experience with private sector expertise at major companies. We deliver custom tailored solutions that drive performance for our partners.
We design and develop products in our R&D center located in United States, serving clients in IVD, medical, and life science markets. Our proven development and project processes always guarantee you transparency to evolve your product successfully to the current and future market needs.
We can help you develop and maintain your Quality Management Systems in accordance with the applicable standards and regulations, including ISO 13485, FDA QSR 21 CFR part 820, 21 CFR part 210/211 and 21 CFR part 4.
We can help you utilize a statistical measure of the inherent process variability of a given characteristic and study to assess the ability of a process to meet specifications.
During a quality improvement initiative, such as six-sigma, a capability estimate is typically obtained at the start and end of the study to reflect the level of improvement that occurred.
Yes, we are available via chat, email and phone 24/7. We have a dedicated line for emergencies as well.
When needed, we can schedule in house trainings on all products we support. We also provide video tutorials and additional resources on our website.
We use the latest technology to secure all information on your business's network. All breaches have multiple layers to get through before any data is accessed.
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