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Each member of the ProceMed executive team has over 20 years of experience within the medical device field, primarily within engineering and sales. We focus on leading the ProceMed team to over-deliver on our promises to each customer.
Our team works within ISO 13485:2016 regulatory environments with PMA, IDE, and 510k Class II and III devices and processes. We will design processes and equipment that match the scope of your product's regulatory filings.
Each member of the team are hands on individuals, who have created devices, products, processes, and value to the organizations where we have worked. We require getting our hands dirty to truly understand the problem and solve it.
At ProceMed , our team includes seasoned veterans having worked from med-device assembler, first employee at start-ups, to business owners. We understand the needs at each level of your business, and work with you accordingly.
Extensive experience in R & D, Process Development, Manufacturing, Regulatory, Supply Chain, and Quality engineering for coronary, neurovascular, peripheral, and ophthalmic Class II & III devices launched and brought to high volume in various worldwide markets.
We have launched large scale manufacturing operations of newly approved products involving thousands of operators, working across all types of product lines in multiple countries. We work with companies from small budget start-ups to multi-billion-dollar corporations and delivering upon their needs.
We specialize in providing cutting-edge process engineering solutions to our clients. Our team of experts is dedicated to delivering quality work on time and within budget. We have full capabilities to create or modify your process, train the team, assist or run validations, and scale up operations to meet your needs.
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