Horus Scientific specializes in histology and pathology services tailored for researchers, toxicologists, and medical professionals across academic, governmental, industrial, and medical sectors. The company offers a range of immunohistochemistry services, employing both established and innovative methodologies to meet client needs. By collaborating closely with clients, Horus Scientific aims to support their specific objectives in research and diagnostics.
T3 Labs specializes in pre-clinical testing and training services for medical devices and biologics, ensuring compliance with Good Laboratory Practice (GLP) standards. The company focuses on enhancing patient care through its comprehensive medical device training programs, which cater to physicians, sales staff, students, and allied healthcare professionals. T3 Labs provides essential resources and facilities for testing and training, allowing these stakeholders to access the necessary tools and knowledge to improve their skills and service quality in the medical field.
Fusion Biotec is a manufacturer of medical instruments focused on the diagnostics and medical device industry. The company specializes in the creation of custom medical devices and complex electro-mechanical diagnostic instruments. By combining art, science, and engineering, Fusion Biotec develops innovative, elegant, and cost-effective medical gadgets that address various healthcare needs.
Kickfile is a provider of compliance technology focused on serving the medical devices, cosmetics, and pharmaceutical industries. The company aims to raise awareness and simplify the compliance process for innovative products entering the market. Kickfile offers a range of tools, including processes, templates, and forms that assist with clinical evaluation, clinical investigation, and post-market surveillance, facilitating the necessary activities to ensure regulatory compliance.
Lea Reg serves as a designated local representative or agent to help medical device and IVD companies meet national regulatory and registration requirements.
Devicia is a full-service clinical research organization specializing in medical devices and in vitro diagnostics. The company provides a range of consultancy services, including expertise in strategy, quality assurance, regulatory affairs, clinical affairs, and biocompatibility. By collaborating with partner organizations, Devicia offers informed perspectives and comprehensive support to clients throughout the entire life cycle of medical devices. Additionally, the organization focuses on medical writing services, enhancing its capability to assist clients in navigating the complexities of the medical device industry.
Limulus Bio is a biocompatibility and toxicology partner for medical devices. It offers Internal and external education in biocompatibility and toxicology for medical devices, as well as conferences.
Clarvin is a healthcare consulting firm that works on regulatory affairs and quality assurance for medical devices.
Medidee is a company that specializes in clinical and regulatory affairs for medical devices. It offers expertise in quality system management implementation and provides clinical compliance services to healthcare institutions. Medidee focuses on various areas, including clinical research, medical data protection, and the transition to in vitro diagnostic regulation (IVDR) and medical device reporting (MDR). By assisting clients with these regulatory processes, Medidee helps ensure that medical devices are approved for use in hospitals and clinics, thereby facilitating their operation and supply in the healthcare sector.
Worrell Design is a design firm focused on healthcare innovation to create better health outcomes.
IMMR is a research is a contract research organization company that conducts and designs biotech and medtech preclinical surgical research. They excel in procedures ranging from early feasibility studies through to GLP studies to support worldwide regulatory approvals. In addition, the company has conferencing facilities and communications capabilities for interactive procedure observation, on-site and remote, real-time, and allowing virtual participation by additional members of your team and for training and demonstration purposes. IMMR was founded in 2003 and is headquartered in Paris, France.
Experien Group offers a comprehensive suite of regulatory, quality, and clinical consulting services specifically for MedTech companies. The company specializes in regulatory affairs, quality systems, as well as pre-clinical and clinical consulting. Additionally, it provides expertise in data management and biostatistics, assisting clients in navigating the complexities of the MedTech landscape. Through its diverse range of services, Experien Group aims to support companies in achieving compliance and enhancing their operational effectiveness within the medical technology sector.
Boston Healthcare is a global strategy consulting firm that focuses on helping clients navigate the complexities of the healthcare landscape. The firm specializes in advising both emerging and established companies in the medical devices, diagnostics, and biopharmaceutical sectors. By developing market access and value optimization strategies, Boston Healthcare assists innovators in capturing the potential value of their products and services. The firm's work aims to transform patient care and enhance health outcomes by facilitating the commercialization of specialized healthcare solutions.
Quartesian is a pharmaceuticals company based in Princeton, New Jersey, specializing in clinical data management services. The company provides a range of offerings including biostatistics, statistical programming, medical writing, pharmacovigilance, and data visualization. Quartesian is focused on delivering customized and insightful data to organizations conducting clinical studies, helping them to effectively manage and interpret their data throughout the clinical trial process.
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