Innovation in
Medical Technology
Committed to Quality and Efficiency
About Medethica
Medical Technology Consulting Experts
Medethica is a medical technology consulting business headquartered in Montreal, Canada that specializes in helping medical technology companies at any stage to validate their products and ideas in clinical settings.
In the realm of MedTech, cutting-edge technologies such as artificial intelligence (AI), remote monitoring, and data collection have emerged as pivotal catalysts. These innovative tools, alongside groundbreaking medical devices, play a pivotal role in diagnosing, treating, and even preventing diseases. Outsourcing has become a strategic approach for medical device companies, empowering them to expand capacity, prioritize growth initiatives, and address any knowledge deficiencies they may encounter.
With a team of experts in medicine, basic research, management, regulatory and technology, we provide business strategy and medical development services to optimize your operations and scale.
We have expertise in study design, clinical trials, protocol writing and ethical compliance. We have a vast network of experts in healthcare institutions in North America and Europe in different specialties to help your company expand and partner with institutions to test and validate products. We also strategize and facilitate the Institutional Review Board (IRB) and protocol design processes.
We hold ourselves up to the highest of standards, and have been part of this industry since 2010. We continue to expand our practices each and every day, and supply many local and global companies with innovative approaches, created with the greatest degree of precision and care.
Consultation Services
Business Development and Partnerships
Consult with experts to strategize partnerships.
We assist companies in identifying strategic partnerships, collaborations, and business opportunities within the healthcare and life sciences sectors.
We provide personalized guidance in evaluating partnership opportunities, negotiating agreements, and fostering relationships with key stakeholders to drive business growth and innovation.
Institutional Review Board (IRB) applications
We assist clients in preparing Institutional Review Board (IRB) applications and protocols for clinical research studies. This involves ensuring compliance with ethical and regulatory guidelines, developing informed consent documents, and addressing IRB feedback to obtain study approval.
Institutional Review Board (IRB) applications
We offer expertise in protocol development, patient selection and recruitment strategies, regulatory compliance, and study execution to ensure successful trial outcomes.
Real-World Evidence (RWE) Generation
Have you developed an AI or digital health solution to address a clinical need and now you need to demonstrate and validate its functionality on clinical data? We assist clients in generating real-world evidence (RWE) to support regulatory submissions, market access strategies, and post-market surveillance. This could involve designing and implementing observational studies, analyzing real-world data, and interpreting findings to inform decision-making.
Clinical Validation and Medical Affairs
We Offer strategic guidance and support in medical affairs activities, including validating a new Med Tech solution (including AI-powered product), medical strategy development, KOL engagement, scientific communications, and regulatory compliance.
We provide expertise in areas such as medical education, publications, and evidence generation to support product development and commercialization of novel products. Our multidisciplinary team of experts will provide practical advice and facilitate the IRB process.