Medical DeviceQualified Supplier Directory
Medical Regulatory affairs and compliance
- Laboratory research services (1)
- Legal counsel (1)
- Market research services (4)
- Marketing, distribution services (1)
- Packaging, labeling services (11)
- Patenting (1)
- Process development and validation (10)
- Product R&D, design (17)
- Product testing- consulting (5)
- Quality systems certification (1)
- Regulatory affairs and compliance (10)
- Research/specimen procurement (1)
- Software design, programming (11)
Viewing ALL listings in Regulatory affairs and compliance
...Management Rapid Design & Development Optical &Imaging, Electrical, Mechanical, Industrial, Fluidics, Test, Software, Firmware Regulatory Guidance & Compliance System Design Rapid Prototyping Verification & Validation Technology Transfer Transitional Manufacturing...
Omnica Corp. Product Development
...and resources. Technical personnel at Omnica includes industrial designers, mechanical engineers, electronic engineers, advanced R&D specialists, regulatory staff, machinists and model makers. Our staff are familiar with FDA documentation and have experience in designing for co...
...Enhancement EMI – EMC Compliance Safety Compliance Fast-track FDA Approval We are experts in the development, design, documentation, and regulatory compliance of new medical devices. Our knowledge of and experience with regulatory requirements, and of the processes needed...
NAMSA is a medical research organization providing expert regulatory, laboratory, clinical, and compliance services to medical device and healthcare product manufacturers. At every stage of the product development process, we provide strategic guidance and tactical support to help...
Collagen Solutions develops, manufactures, and supplies medical-grade collagen biomaterials for use in research, medical devices, and regenerative medicine. It partners with its customers by providing quality biomaterials along with regulatory and technical expertise to develop and...
Donawa Lifescience Consulting Srl
DLC, headquartered in Rome, Italy, and founded by a former US FDA CDRH official who serves as President of the company, is a regulatory and quality system services consulting firm and full service contract research organization (CRO) for medical devices, including in-vitro diagnost...
JKS & Associates
Contact: John Suzuki Year Established: 1993 No. of Employees: 2 Key Clients: Pfizer, Integ, Ohmeda, Liebert (Emerson Electric), Xerox, IBM Global Services, AMO, Cordis, Alcon. JKS & Associates provides cost-effective software consulting for small and large manufacturers in requi...
MakroCare, an international management consulting services firm, supporting global clients through its 5 divisions - Consulting, Commz, CRO, SMO, and Informatics. Offering services in regulatory affairs, risk management, regulatory compliance, clinical trial management, biometrics,...
NEO Tech (NEO Technology Solutions)
NEOTech combines the strengths of three leading contract manufacturers: NATEL, EPIC, and OnCore. NEOTech serves the medical, defense/aerospace and industrial markets. NEOTech offers product engineering services, manufacturing and testing of microelectronics, cable & harness, PCBA...
Tecno-med Ingenieros is a consultancy company located in Barcelona, Spain. Our goal is to provide regulatory support and expert advice for manufacturers, importers, distributors and exporters of medical devices as well as all associated service providers. We are specialists in the...