Is your medical device or digital health company facing regulatory hurdles, clinical trial challenges, or quality assurance complexities? HaMaDa Consulting offers the expertise you need to navigate these complexities and accelerate your path to market.
For over 16 years, we’ve partnered with over 300 clients, providing comprehensive support across the entire product lifecycle. Our team of 25+ highly skilled consultants possesses unparalleled expertise in a wide range of medical fields and technologies. We help you:
- Streamline Regulatory Affairs:Â Seamlessly navigate FDA, CE, and global regulatory requirements with our expert strategies and submissions.
- Conduct Efficient Clinical Trials:Â From study design to data management, we ensure efficient and compliant clinical studies.
- Ensure Unwavering Quality:Â Meet and exceed ISO 13485, MDR, IVDR, MDSAP, and FDA-QSR standards with our comprehensive QA/compliance services.
- Write Effectively:Â Our experienced medical writers craft compelling submissions and publications that resonate with regulators and healthcare professionals.
We’ve worked with industry leaders such as Omrix Biosurgery Israel, Applied Spectral Imaging (ASI), GynTools, and we’re ready to help you achieve your goals.
Connect with us today to discuss your specific needs and discover how HaMaDa can help you achieve breakthrough results!
