FDA Investigator: Lauren M. Lilly
- Lauren M. Lilly first started conducting FDA inspections in 2018, with the last inspection in 2023. Over that time, Lauren M. Lilly has conducted 42 inspections at 31 companies across 42 sites.
Get Lauren Lilly's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.
Documents
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FDA 483 Abraham J. and Phyllis Katz Cord Blood Founda | 2023
Available Now - $199
Lauren M. Lilly
Biologics Form 483
FDA 483 Predictive Biotech, Salt Lake City | June 2021
Available Now - $199
Lauren M. Lilly
Biologic Form 483
FDA 483 MD Anderson Cord Blood Bank, Houston | 2022
Out-of-stock
Lauren M. Lilly
Biologic Form 483
FDA 483 Grifols Diagnostic Solutions Inc, San Diego | 2022
Out-of-stock
Lauren M. Lilly
Biologic Form 483
FDA 483 Par Sterile Products LLC, Rochester | 2021
Out-of-stock
Lauren M. Lilly
Biologic Form 483
FDA 483 Brammer Bio MA, LLC, Cambridge | 2021
Out-of-stock
Lauren M. Lilly
Biologic Form 483
FDA 483 Brammer Bio MA, LLC, Somerville | 2021
Out-of-stock
Lauren M. Lilly
Biologic Form 483
Co-Investigators (19)
- Nancy L. Neiger, FDA Investigator
- Darla J. Christopher, FDA Investigator
- Gene D. Arcy, FDA Investigator
- Linda Thai, FDA Investigator
- Susan M. Jackson, FDA Investigator
- Richard L. Bartlett, FDA Investigator
- Laurissa S. Flowers, FDA Investigator
- Steven E. Bowen, FDA Investigator
- Scott T. Ballard, FDA Investigator
- Kanaeko R. Ravenell, FDA Investigator
- Kunapuli T. Madhusudhan, FDA Investigator
- Frans E. Mercado, FDA Investigator
- Shannon A. Lowe, FDA Investigator
- Susan M. North, FDA Investigator
- Elmina E. Akwo, FDA Investigator
- Aneel K. Sandhu, FDA Investigator
- Decarlos A. Gomez, FDA Investigator
- Nimmy Mathews, FDA Investigator
- Jonathan A. Womack, FDA Investigator