Inspection Readiness and Regulatory Compliance 2024 – San Diego Workshop Tablet Image Inspection Readiness and Regulatory Compliance 2024 – San Diego Workshop Mobile Image
Mobile Gradient

Inspection Readiness and Regulatory Compliance 2024 – San Diego Workshop

Thursday, May 2, 2024

Inspection Readiness and Regulatory Compliance 2024 – San Diego Workshop Tablet Image Inspection Readiness and Regulatory Compliance 2024 – San Diego Workshop Mobile Image
Mobile Gradient

Inspection Readiness and Regulatory Compliance 2024 – San Diego Workshop

Thursday, May 2, 2024

 
Home /

Our compliance team has seen enough to insist that clinical study inspections are not a question of “if”, but of “when”. However, true inspection-readiness is hard to achieve, especially if it’s your first one.

What do sponsors say about the Inspection Readiness Workshop?

“YES, absolutely useful! Especially the suggestions for good hygiene (to be prepared for an audit). For example, the suggestion to have a Data Map or Storyboard created to refer to”
Director, Clinical Operations
“The slides detailing areas that you notice the FDA has been focusing on recently were very valuable.”
Executive Administrator
“My background is in IRT. The one thing that was informative to me was that Almac creates an inspector role within the IRT”
Clinical Supply and IRT Support Manager
“It was very informative and provided a lot of “helpful hints” and important points to consider. I particularly enjoyed the round table discussions afterward when we all shared our experiences with Almac CT, as well as other IRT providers. Great opportunity to share.”
Clinical Trial Supply Study Manager
“I found the program very current, targeted, and educational. I found the discussion around storyboards particularly useful and the Q&A discussion with real-life examples of issues around the IRT put things nicely in context.”
Executive Administrator

Please join us at the San Diego installment of Almac Clinical Technologies’ most informative and insightful regulatory workshop series of the year to learn how to stay ahead of audits and how your IRT vendor can help you do it. 

Almac’s Matt Lowrie who in his role as a Quality and Assurance Manager has overseen hundreds of inspections will share his “dos and don’ts” playbook for Sponsors and answer any of your questions to help you be better prepared.

Location: Skybox at DiamondView Tower, 350 Tenth Ave, San Diego, CA

Date: Thursday, May 2, 2024

Workshop and Q&A session: 2:30pm-4:00pm

Cocktails and hors d’oeuvres: 4:00pm

Who should attend?

Clinical Trial, Clinical Operations, and Clinical Supply Managers; Quality and Assurance teams

Registration

To secure your place at this exclusive workshop, please complete the registration form.  Spaces are limited, so make sure to reserve your place as soon as possible.

*By submitting your information you acknowledge that you have read the privacy statement and you consent to our processing the data in accordance with that privacy statement. We may, from time to time, send you material relevant to your interests. If you change your mind at any time about wishing to receive material from us, you can send an email to [email protected]. Every email we send you will also include an unsubscribe link so you can unsubscribe from our marketing list.

Speakers

Matt Lowrie

Matt Lowrie

Manager QA & Regulatory Compliance, Almac Clinical Technologies

This website uses cookies. By continuing to browse the site, you are agreeing to our use of cookies