At HLR Bio, biotech research and development, with a particular focus on In Vitro Diagnostics (IVD). Our aim is to support the development of innovative and efficient diagnostic tools that can revolutionize healthcare.
Our partnerships with other biotech companies and research institutions are expanding, allowing us to leverage more resources and expertise. We are also investing in advanced technologies to enhance research capabilities and speed up the development process.
We want to help you solve your current challenges such as regulatory complexities, data analytics, automation, and high R&D costs. To mitigate these, we can help you explore various options with a committment to maintain strict compliance with all relevant regulations.More...
George Anello
Director of Quality Assurance & Regulatory Affairs@MedDevice Quality Experts
Verified
MedDevice Quality Experts continues to maintain its high standards in Quality Assurance and Regulatory Affairs. We have successfully implemented new quality assurance protocols, leading to a decrease in product defects and an increase in overall product quality. Our regulatory affairs team has effectively navigated recent changes in industry regulations, ensuring our full compliance. We are also improving our risk management strategies, focusing on proactive measures. Our commitment to continuous improvement and adherence to regulatory standards position us well for future growth and success. FDAQSR and ISO 13485 expert.More...