Download →
← All resources

Q&A with the FDA on CSV Changes

Question & Answer session with the FDA on CSV changes. Learn from the FDA & our subject matter experts today!

Q&A with the FDA on CSV Changes
Webinar

Watch this webinar

Question & Answer session with the FDA on CSV changes. Learn from the FDA & our subject matter experts today!

Fill out the short form and scroll down to access the full content.

We only use your details to deliver this download and follow up on your request. No newsletter detour. Unsubscribe anytime.

Agree to Privacy Policy and Email Opt-In *

By submitting this form, you agree to USDM’s Privacy Policy and consent to receive communications from USDM. You can unsubscribe at any time using the link in our emails.

This on-demand webinar discusses the upcoming CSA guidance and how life sciences companies can and should be applying the principles and methodologies today.

USDM hosted a webinar, Update from the FDA on CSV Changes, with Francisco Vicenty, Case for Quality Program Manager, FDA, discussing the upcoming Computer Software Assurance (CSA) guidance and how life sciences companies can and should be applying the principles and methodologies today. Due to the overwhelming amount of questions we received from 2,000 of your peers, we created this follow-up webinar to answer the many questions we couldn’t address in time.

Join our exclusive Q&A session with Francisco Vicenty to hear questions answered from across the life sciences industry on CSA. You can read the questions and answers on this blog post.

The discussion will include:

  • Live Q&A
  • What changes to CSV will impact you
  • Deeper dive on what CSA means to you

About the Presenters

Francisco Vicenty, Case for Quality program manager, the U.S. Food and Drug Administration

Cisco Vicenty is currently the Program Manager for the Case for Quality (CfQ) within the Office of Product Evaluation and Quality, Center for Devices and Radiological Health (CDRH), FDA. The Case for Quality has been a strategic priority to improve device quality, access, and outcomes for patients. Cisco has worked as a manager within compliance at CDRH and previously worked in quality and reliability within the semiconductor industry.

Sandy Hedberg, Cloud Assurance QA/RA manager, USDM Life Sciences

Sandy Hedberg has over 20 years of experience in Quality and Regulatory Affairs in the medical device, pharmaceutical, and biologics industries. She has participated in assisting companies with responses to consent decrees and audit findings to the FDA. She is well versed in risk analysis, creation of quality procedures, computer system validation, auditing, and authoring regulatory submissions.

Additional CSA References:

You can also download our datasheet for more information on CSA.

Watch the webinar

Fill out the short form above to access the complete download.

Watch the webinar

Explore capabilities

Find the USDM practice area most relevant to this topic.

Platform partners

See how USDM delivers outcomes on the platforms you use.

Continue the conversation

Apply these insights to your organization.

Take the next step after this session. USDM can help you scope, validate, and execute the strategies discussed — inside your GxP environment.

  • Expert-led assessment of your current state
  • Regulatory context mapped to your specific systems and workflows
  • Prioritized roadmap based on risk and business value
  • US and EU delivery presence with active regulatory experience

Continue the conversation

Speak with a USDM specialist

Take the next step after this session. Our team can help you apply these insights to your specific regulatory context.

Agree to Privacy Policy and Email Opt-In *

By submitting this form, you agree to USDM’s Privacy Policy and consent to receive communications from USDM. You can unsubscribe at any time using the link in our emails.