They Regulate We Understand
Navigating regulatory hurdles, solving your compliance challenges, accelerating your medical device success.
About Us
At V-Reg Solutions, we pride ourselves on our commitment to honesty, ensuring transparent communication every step of the way. With a focus on on-time delivery, we navigate Medical Device Manufacturers through regulatory processes efficiently, never compromising quality for speed. Our team consists of expert individuals who approach each project with a risk-based mindset, ensuring thoroughness while minimizing delays. Welcome to a consultancy where passion, collaboration, and dedication merge to propel you toward unprecedented success.
About Our Service
Our team goes beyond document creation, offering tailored assistance throughout your application journey, providing guidance on classification, validation, testing, and addressing regulatory agency inquiries to ensure a smooth process.
Sign an Annual Contract with us for comprehensive Quality Management support. We'll update your reports, rewrite clinical and risk documents, monitor standards, conduct pre-audit visits, and assist wi...
QMS Maintenance Contract
Empower your team with comprehensive Medical Device Regulatory Trainings tailored to ensure compliance and excellence. Our expert-led courses provide essential knowledge for navigating complex regulat...
Regulatory Trainings
At V-Reg Solutions, we specialize in maintaining design and development files, crucial for regulatory compliance. Our expert team conducts research, creates verification and validation plans, selects ...
Design and Development
Our expert team ensures smooth navigation through regulatory requirements, helping your products reach the market efficiently. Trust us to streamline your CDSCO registration journey.
CDSCO Registration
At V-Reg Solutions, we provide guidance for classification, validation, and regulatory inquiries. Trust us for services like Technical File Construction, Clinical Evaluation Report Preparation, and Ga...
Regulatory Affairs
Our services cover the entire spectrum of clinical evaluation requirements for medical devices. From developing essential documents like Clinical Evaluation Plans (CEP) to compiling reports such as Po...
Clinical Evaluation Support Service
Simplify ISO 13485 compliance with our SOP and format preparation and implementation services. We tailor documentation to your needs, ensuring seamless adoption and adherence to regulatory standards f...
QMS Documentation and Implementation
Simplify country-specific registration compliance with V-Reg Solutions. We ensure documentation aligns with each country's regulations, facilitating smooth adoption and regulatory approval for market ...
Country Registration
Our Clients
Trusted by leading organizations in the medical device industry, we are proud to work with these esteemed companies in delivering regulatory compliance and quality solutions worldwide
Let's bridge the gap between regulations and excellence! Connect with us to unlock a concept designed to streamline your operations.
