Sigal is an accomplished entrepreneur and idea originator with extensive experience in the gastro medical device sector. She successfully led an Israeli gastro medical startup through a significant transformation into a US-based public company, culminating in a successful Nasdaq IPO. Her expertise encompasses operations management, engineering, and patent filing, ensuring strict compliance with FDA regulations and ISO standards. Additionally, Sigal's strong financial planning skills have been instrumental in securing funding and effectively managing budgets. With both a Master of Public Administration (M.P.A.) and a Master of Business Administration (M.B.A.), she combines her educational background with practical experience, positioning herself as a key player in the gastro medical device industry.

Nir has extensive experience in both startups and small to medium-sized enterprises (SMEs), where he excels at combining agility with hands-on problem-solving skills in fast-paced development environments. He is a recognized expert in prototype development, proof of concept, software algorithms, and lab trials, making him a valuable asset to any team.

With a Bachelor of Science in Electrical and Electronics Engineering, Nir possesses a solid technical foundation that supports his innovative contributions. His knowledge of ISO 13485 standards ensures quality and compliance in all his projects. 
 

Anat is a highly skilled specialist in building effective cross-functional and international partnerships. With extensive experience in project management and leading full product lifecycles, she excels at translating customer needs into innovative solutions across various tech sectors, including submissions.

Her strong analytical skills allow her to identify market trends and customer requirements, ensuring impactful solutions. Holding a Bachelor of Science in Chemical Engineering and a Software Engineering Diploma, Anat combines technical expertise with strategic.

Orit brings extensive experience in global clinical trials, regulatory affairs, and quality assurance to Tenasors. With deep expertise in FDA submissions, ISO 13485 standards, and CE Mark processes, she is adept at navigating the complex healthcare regulatory landscape.

Her comprehensive background enables her to effectively manage the challenges associated with clinical trial protocols and regulatory compliance, ensuring that products consistently meet rigorous international standards. Orit holds a Master of Science in Drug Regulatory Affairs and a Master in Public Health, providing her with a strong understanding of both the scientific and regulatory aspects crucial for success in the industry

Alexander is a seasoned professional with extensive experience in leading New Product Introduction (NPI) processes, including the management of Document History Records (DHR), Design Master Records (DMR), and Design History Files (DHF). He has a proven track record in creating Bills of Materials and writing maintenance instructions, as well as developing test procedures and OQ/IQ protocols for electromechanical test jigs. 

In addition, Alexander is skilled in managing Engineering Change Orders (ECOs), ensuring smooth transitions and updates in product specifications. He has also provided support for clinical trials, maintaining comprehensive documentation for the FATIGUE/AWT lab.