Virant Diagnostics is able to play a pivotal role in collaborating effectively with pharmaceutical and biotech companies, throughout various stages of clinical development following the FDA regulatory process, by offering a comprehensive suite of services tailored to support their unique clinical trials and research endeavors.
As a central laboratory partner, we bring a wealth of expertise in clinical diagnostics, specimen management, and regulatory compliance. Our state-of-the-art facilities are equipped with cutting-edge instrumentation and staffed by experienced professionals who ensure the highest standards of accuracy and precision in data generation. We understand the critical nature of timely and reliable results in drug development, and our commitment to quality and efficiency aligns perfectly with the needs of our industry partners.
We understand the importance of a central laboratory in standardizing and ensuring the quality and consistency of data generated across multiple trial sites, contributing to the reliability of clinical trial outcomes and drug and device development decisions. We adhere to stringent regulatory guidelines, including Good Clinical Laboratory Practice (GCLP) and Good Laboratory Practice (GLP), to maintain the integrity and traceability of the data they generate for pharmaceutical companies by being ready to contribute to the success of pharmaceutical and biotech companies, ultimately advancing healthcare and improving patients’ lives.