We understand the importance of your viral clearance study, which is why we are committed to providing a flexible and high quality service. While we handle all the work, you get full transparency, control, and insight into every aspect of the study.
Our Provise™ Clearance Service deploys a team of highly trained & experienced process scientists and study directors on your behalf, to perform all your required process steps at our state-of-the-art facilities. We will communicate with you to inform you at every step without the need to leave your workplace, maximizing your team’s productivity. You will receive a QA-audited final report to expertly support your regulatory filing.
Our dedicated team leverages extensive experience in:
Your dedicated process team will perform all viral clearance steps on your behalf, keeping you up to date with progress of your study. You will receive a final report and support through your regulatory journey, all while you are doing value-added work within your own facility.
In this paper, we will share how to ensure your manufacturing process has the capacity to remove or inactivate enveloped and non-enveloped viruses.
Learn how our experts, with decade of experience, help design and execute your clearance studies.
Discover key numbers on our experience with viral clearance studies.
Discover how we can do your viral clearance studies for you, keeping you informed along the way.
Read about key factors to consider for virus inactivation steps or model virus panels for your AAV clearance study.
In this webinar, you will learn about key updates in the ICH Q5A (R2) and how these may impact virus clearance study design.
Learn about important viral clearance study considerations when transitioning to continuous processing.
In this webinar, you will learn strategies for ensuring the viral safety of novel therapies.
In this webinar, we discuss potential issues that can arise during viral clearance study design and execution, and strategies to mitigate risks.
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