"AKRA TEAM covers it all! Over the last two years, we have benefitted from clear MDR guidance and wise counsel that has enabled us to navigate clinical expert panels, complicated post-market clinical follow up, derogations, drug dossiers, and everything in between." August 2023

"CROMA engaged with Bassil Akra and Team for MDR compliance projects. He supported us in understanding the critical steps towards MDR certification and bringing class III combination devices to MDR CE. His experience and knowledge was very supporting both in delivering for practical clinical work packages and templates as well as in strategic communication with the notified body. I appreciate Bassil´s approach in being always accessible, pragmatic and straight forward delivering results. Less general talking more outcome, that is how consultancy should be. Thank you again AKRA TEAM for your support." November 2023

"AKRA TEAM came to the rescue with a complex and protracted clinical evaluation of high risk medical device softwares. We highly appreciate Bassil’s enormous knowledge of the relevant guidelines and regulations, his personal support in our communication with the Notified Body, and his team’s effort in reviewing CEP, CER, SSCP, and PMCFP, all of which was done in a thorough, precise, and timely manner. MED-EL is very satisfied with the results and wholeheartedly recommends AKRA TEAM to anyone needing consultation in tricky MDR issues." January 2024