About our company
Titans Medical Consulting is a partner of choice for medical device regulatory consulting in key markets across the globe. From helping our clients understand the regulatory landscape and making market entry accessible, our team supports with critical regulatory assessment along with technical experience and expertise.
We are a team of over 100 medical device experts based out of the US, Germany, Singapore, and India. We specialize in regulatory consulting for medical devices, In vitro Diagnostics (IVDs), and Combination devices. We offer dependable regulatory consulting for all aspects of your medical devices.
Our Mission
At Titans Medical, We empower and accelerate innovation in the medical device industry by providing comprehensive guidance, strategic solutions, regulatory expertise, and authorization of the product.
Our Vision
We strive to ensure that safe, effective, and innovative medical technologies reach patients worldwide.
Give us a call and speak with one of our consultants. We’re sure they’ll be able to help you with making your regulatory assessment and your market access journey in a comprehensive way.
Greetings from Titans Medical Consulting Team!
Our core idea in establishing Titans as a medical device focused regulatory consulting firm was to ensure we provide a platform for global medtech companies and startups gauge regulatory guidelines and market entry landscape in different countries. Along with helping customers in understanding the regulatory requirements to supporting them make submissions to the health agencies effectively is where we act as a supporting team.
In our journey so far we have supported multiple medtech companies in successfully registering their devices and diagnostic test kits in various countries and ensured market access seamlessly In a definite budget and timeline. We thank you for giving us the opportunity to assist in your regulatory requirements and acting as a key liason to your team in achieving regulatory compliance.
Mrs. Saloni Vig
Mr. Ram Modi
Our Services
We're here to assist, providing guidance throughout the entire journey.
The Central Drugs Standard Control Organization (CDSCO) is the regulatory authority responsible for regulating pharmaceuticals and medical devices in ……
Welcome to Titans Medical’s comprehensive guide on Software as a Medical Device (SaMD), a dynamic and transformative force in modern healthcare. SaMD refers to ……..
– America
– Asia Pacific
– Middle East and Africa
– Europe
At Titans Medical, we understand the critical importance of medical device testing and compliance. Our dedicated team of …….
If you intend to market your medical devices in Europe, it is imperative to create and uphold a Clinical Evaluation Report (CER) that aligns ……