The Global Regulatory Experts Medical Device Compliance Leaders
ISO Compliance and ISO Standards: ISO is a set of global quality standards that are geared to companies providing products or services as a framework for achieving customer satisfaction through implementing a quality management system. The ISO set of standards have become an important mechanism to allow companies to inform their...
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Natech Plastics is an ISO 13485 and 9001-certified provider of product development, custom injection molding, and contract manufacturing services. We also specialize in design for manufacture and scientific molding services, which ensure streamlined schedules and more stable processing for...
The Realtime Group is a software and electronics design and validation testing firm with small business diversity yet certified to ISO13485:2003 for providing software validation, independent verification and validation, and design solutions related to government IT, medical devices, wireless...
The IMSM team work towards a common goal, to consistently deliver to clients world class ISO consultation, reinforced by adherence to our Missions, Visions and Values. At each stage of your product’s life, regulatory requirements are scrutinized in the manufacture, delivery, or service stages....
Virtual Cert™ ASRP Program™: The reason for developing this program is simple: to save our customers thousands of dollars annually and top manager’s valuable time.
We realize in today’s market place, the value of ISO 9001 certification varies from company to company, for some it is a requirement to do business, for the...
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ISO Consultants: ISO 9001, AS9100 & Other Standards Consulting and Internal Audits At my ISO Consultants, our dedicated, multilingual team of experts work together to deliver solutions that will make getting ISO certified simple and painless for you, your employees, and your business. We serve...
European Authorized Representative for MDs and IVDs MediMark Europe specializes in supporting medical device companies to navigate the complexities of the European regulatory landscape, ensuring compliance with crucial EU directives for medical devices and in vitro diagnostic regulations...
Medical Technology Promedt Consulting GmbH, established in 1995 and headquartered in St. Ingbert, Germany, offers a full spectrum of regulatory consultancy services for the healthcare industry, specializing in medical devices, in vitro diagnostics, pharmaceuticals, and biotechnologies. As an EN...
Secure BioMed Evaluations is your expert partner in seamlessly bringing medical devices and biologics to market with accelerated confidence. As an extension of your team, we specialize in comprehensive regulatory strategy and quality management, including document control, internal audit...
Provides consulting and training for medical device and other FDA & Internationally regulated healthcare related industries. Noblitt & Rueland provides expert regulatory consulting and training services tailored for the medical device industry, bringing over 25 years of specialized experience...
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