Knowledge Center

Galway City, Republic of Ireland - January 4, 2024 –

 

The joy at Med-Di-Dia Ltd is palpable as we proudly announce our latest feat - clinching the coveted title of Best Medical Compliance Consultants 2023 in the Republic of Ireland. Following our stellar win as the Best Medical Regulatory & Quality Compliance Consultancy Firm 2022, awarded by Global Health & Pharma, this recognition reaffirms our commitment to excellence in the dynamic landscape of the health and pharma industry.

 

At the heart of Med-Di-Dia's success is the unwavering dedication to "Driving Innovation to Market Success," a philosophy deeply embedded in the ethos of our sister company, Global Regulatory Services (GRS).

 

Mrs. Greer Deal, Director and Co-Founder of Med-Di-Dia Ltd, expressed her delight, stating, "We are thrilled to receive the Global Excellence Award for Best Medical Compliance Consultants 2023 in Ireland. Our team's dedication to ensuring the availability of safe and compliant medical devices is truly commendable. We pride ourselves on caring for every entrepreneur and company, guiding them through regulatory requirements to develop high-quality, safe, and effective devices for those in need."

 

Adding to the excitement, Mr. Bobby Deal, Co-Founder of Med-Di-Dia Ltd, remarked, "This achievement is a testament to our team's hard work and passion. We are proud to be at the forefront of shaping the future of regulatory compliance in the MedTech industry."

Based in Platform94 in the vibrant Galway City, Republic of Ireland, Med-Di-Dia operates alongside its sister company, Global Regulatory Services (GRS), to provide comprehensive support to the broader life science industry.

 

As we bask in the glory of this achievement, Med-Di-Dia remains dedicated to serving as a Regulatory and Quality Risk Partner for Medical Devices, Diagnostics, and Digital Health. Here's to a year of continued success and growth, and positively impacting the health and well-being of communities worldwide.

Medical Device Manufacturers can contact us for end-to-end regulatory and quality compliance support. Our experts are navigating the regulatory maze in the EU, UK, USA and rest of the world where we provide services like:

• European Union Authorised Representative [EU AR]
• Person Responsible for Regulatory Compliance [PRRC]
• US Agent
• UK Representative
• Quality Management Systems
• Market Access and Regulatory Strategies
• Adhoc Regulatory Support
• Much much more….

Reach out to our experts by sending an email to mdd@mddltd.com or by filling out this webform - https://med-di-dia.com/contact.php