Whether you are looking for a reliable genetic analysis partner for patient stratification or an experienced GLP qPCR laboratory for your gene therapy safety study, Avance Biosciences™ offers our experience and expertise to ensure the success of your project. With its broad breadth of service platforms and industry most experienced scientific team, Avance Biosciences™ offers our clients worldwide custom solutions to support their preclinical safety studies and clinical trials. We are committed to full adherence to GLP and CGMP regulations and guidelines promulgated by US FDA (21 CFR Part 58 and 21 CFR Part 210/211), OECD, European Commission (EC), and Japanese agency, as applicable to the service provided.
Avance Biosciences™ offers Sanger sequencing, qPCR, and other “Gold Standard” methods for testing clinical trial samples (such as SNP detection) or validating assays to be used in clinical trials.
We are dedicated to timely, high-quality service from the start of your project to the finish. Send us a note or give us a call to find out what Avance can do for you.
From the preliminary conclusion of this work, we are already pleased to thank you for your customer-oriented approach and proactive communication in the course of this study. We are happy to see the profound difference in business mindset between your organization and our previous vendor…
Project Manager, Belgium
Thank you so much for successfully completing this important project for us on time. We are very satisfied with the final report and thank you for taking the extra effort to customize the report format. We will definitely use your lab for future projects.
Program Manager, California
It has been a pleasure working with you and your team. The project was carried out to the highest standard and delivered in a timely manner. I will definitely recommend Avance Biosciences™’ services to colleagues and friends.
Senior Scientist, Singapore
When you partner with Avance Biosciences™, you gain a CRO partner that is creative, collaborative and dedicated to sound science with a focus on the regulatory requirements our partners require. Contact our technical staff to discuss how we can support you in your project!
Dedication to Quality
The Avance Biosciences™ team is committed to strict adherence to CGMP and GLP regulations enacted by the US, European, Japanese, and other international regulatory agencies.
Our team has extensive knowledge and experience working with scientists, QA/QC professionals, and project managers from over 100 pharmaceutical and biotechnology companies and organizations throughout the world.
Transparency and integrity are two of our core values. Our well-trained, friendly, and professional study directors and project managers strive to complete your projects on-time with open communication channels and to your specifications.
Avance Biosciences™’ CGMP/GLP compliant genomic and microbial assays make use of the advanced technologies including real-time PCR, ddPCR, Sanger sequencing, next-gen sequencing, Southern blot, and more.