Working with Dr. Priyanka Murawala has been absolutely invaluable for our company. Her expertise in biocompatibility under MDR allowed us to efficiently meet complex regulatory requirements. Dr. Murawala demonstrated not only deep professional knowledge but also exceptional analytical skills and attention to detail.
Her professional approach, quick responses, and ability to clearly communicate complex information saved us time and effort while providing confidence that our documentation fully complies with all requirements. I wholeheartedly recommend collaborating with her to any company working with medical devices and seeking to ensure full compliance with European regulations. Thank you, Dr. Murawala, for your help!
Dr. Murawala has been an invaluable partner in supporting us with our biocompatibility needs. She provided thorough guidance on the best biocompatibility strategy for our device. Her deep knowledge of the applicable regulations, along with strong connections to testing laboratories, ensured a comprehensive compliance solution. We highly recommend Dr. Murawala and Eunoia Compliance for their expertise and professionalism.
Dr. Murawala’s biocompatibility expertise has been instrumental in the success of Inari Medical’s development of the LimFlow technology. She is a reliable partner in helping to define sound biocompatibility strategies across various device types, indications, and regulatory environments. Highly recommended.
“Dr. Murawala is our biocompatibility expert and an important part of our development team. She is very responsive and thorough in helping us determine the best biocompatibility strategies for our devices and documenting the results in our Biological Risk Assessments.”
“I have had the privilege of working closely with Priyanka M. on multiple medical device development projects, where her expertise in biocompatibility assessment proved invaluable. She possesses an exceptional understanding of biological evaluation frameworks, particularly ISO 10993 and related regulatory expectations across global markets.”
“I have been collaborating with Priyanka, the owner of Eunoia Compliance, for many years—initially when we were both employees at a medical device manufacturer, and now also as fellow consultants. As a medical device regulatory affairs consultant, I deeply appreciate Priyanka’s exceptional subject matter expertise and her ability to quickly understand and address her customers’ needs.
Priyanka’s extensive experience spans various medical device applications, including devices with different types of body contact and durations as categorized by ISO 10993-1. Her strong connections with testing laboratories further enhance her ability to deliver tailored solutions. Moreover, her in-depth knowledge of both EU MDR requirements, including interactions with notified bodies, and US FDA regulations ensures a comprehensive approach to compliance.
For any medical device developer or manufacturer navigating the complexities of regulatory compliance, I highly recommend Eunoia Compliance and Priyanka’s expertise”
Priyanka is our go-to resource for all things related to biocompatibility, from early material selection and risk assessment through formal testing. She is easy to work with, well organized, extremely responsive, and uniquely creative when it comes to handling the difficult challenges that arise in medical device development. I highly recommend Eunoia Compliance.
“I highly recommend Priyanka and Eunoia compliance. She got up-to-speed very quickly and provided us with a cost-effective thorough assessment and expert guidance.”
“Dr. Priyanka Murawala is a consulting Biocompatibility SME on our team and she has been instrumental in our success in achieving compliance with her deep subject matter knowledge, detail-oriented approaches and problem-solving capabilities. Highly recommend Dr. Murawala!”
