Expansion Announcement: Strengthening Med-Di-Dia's Regulatory Expertise
Since our inception in 2019, Med-Di-Dia has remained committed to reducing regulatory complexities and burdens for MedTech manufacturers globally. Our unwavering mission has been to support the Medical Devices, Diagnostics, and Digital Health sectors in achieving compliance with stringent regulations across the EU, UK, USA, and worldwide.
To further empower our mission, we are thrilled to announce a pivotal expansion of our team. Dr. Shahram Ahmadi and Jacob Skinner have recently joined Med-Di-Dia as Regulatory and Quality Compliance specialists. This addition significantly bolsters our capabilities, allowing us to provide end-to-end support for regulatory compliance, ranging from strategic report to post-market vigilance. Med-Di-Dia, in collaboration with our sister company, Global Regulatory Services (GRS), is ready to assist you in navigating the MedTech regulatory landscape across the EU, UK, USA, and the rest of the world.
Contact us by email at firstname.lastname@example.org to book a FREE 30-minute consultation with our team members.
Introducing Dr. Shahram Ahmadi
Dr. Shahram Ahmadi is a seasoned Regulatory Affairs and Quality Assurance Specialist, bringing 14 years of invaluable experience to our team. His expertise encompasses a wide spectrum of medical device categories, including implants, Personal Protective Equipment (PPE), and dermatological products featuring medicinal components. Shahram's proficiency shines through in his commitment to implementing ISO 13485:2016-compliant Quality Management Systems, developing Standard Operating Procedures (SOPs), and efficient audit management.
Notably, Shahram has been a steadfast representative of Med-Di-Dia, actively participating as a speaker and delegate at various industry events, such as NSL Days, Medical Technology Ireland, and The Future of Swedish & Danish Life Science. He continues to be our distinguished ambassador in the Nordic Region.
Meet Jacob Skinner
Jacob Skinner assumes the role of Medical Device Regulatory Affairs and Quality Assurance Consultant at Med-Di-Dia. With a five-year background in UK and European Regulatory Affairs, he specialises in delivering comprehensive regulatory support to MedTech companies and medical device manufacturers. Jacob's expertise encompasses regulatory strategy and planning, ISO 13485:2016 Quality Management Systems integration, and medical device classification services. He holds a BSc(Hons) degree in Human Biology.
Jacob's commitment to regulatory excellence extends to his representation of Med-Di-Dia at notable industry gatherings, including the Medilink Expo and the NHM Compliance Conference. Moreover, he recently published a paper in collaboration with the Regulatory Affairs Professional Society (RAPS) on "Medical device regulation in the UK,” which highlights his dedication to advancing industry knowledge.
You can request a copy by visiting - https://lnkd.in/eNWWY4uE
As our team continues to expand, we reaffirm our commitment to offering free resources for the development of Regulatory Affairs and Quality Assurance in the MedTech sector. Whenever manufacturers require support, we are ready to provide our comprehensive services for achieving end-to-end regulatory and quality compliance.
Feel free to get in touch with us to navigate the complex regulatory landscape with confidence and support. Reach us via email at email@example.com or complete our interest form: https://mailchi.mp/8e91e0f1dba0/c3prlu9zgy
Med-Di-Dia – Your Trusted Partners in Managing Regulatory Risks for Medical Devices, Diagnostics, and Digital Health!