FDA Investigator Lauren M Lawrance

Lauren M Lawrance has conducted inspections on 155 sites in 3 countries as of 13 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
155
Last Inspection Date:
13 Jun 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America, Germany, Switzerland
FDA Investigators that have inspected at least one site in common with Lauren M Lawrance:
Abby E Pelletier, Alan R Condon, Aldo J Quintana, Alfred P Pistorio, Alice C Silva, Alissa E Berryman, Allison A Rodriguez, Almaris N Alonso, Alois P Provost, Althea A Williams, Alysia M Salonia, Amber G Wardwell, Amy C Jordan, Amy M Cramer, Andre S Lamontagne, Andrew M Barlow, Andrew P Abban, Anne E Carpenter, Anthony P Costello, Anthony W Thomas, Ashley M Whitehurst, Atricia L Irons, Bradford L Swanson, Bradley D Newsad, Brenda P King, Byungja E Marciante, Carla C Cummins, Carla C Tuite, Christine L Williams, Christopher A Demitrius, Christopher K Vantwuyver, Christopher M Elliott, Courtney N Long, Darin S Wiegers, David J Feria, David M Lamoureux, David P Vanhouten, Dawn M Braswell, Diane M Biron, Dominic R Frasca, Donahue, Donna J Clevenger, Dorothy W Lee, Douglas S Joslin, Eduardo L Rodriguez, Edward J Janik, Elise L Mcdevitt, Elizabeth B Griffin, Emily J Schramm, Eric C Schmitt, Erich P Garger, Erin P Conlin, Frank J Koch, Frank J Marciniak, Frank K Fulford, Gale E Ryan, Gary J Hagan, George T Allen, Jr, Gerard D Difiore, Guozhou Mo, Hien Albright, Intkhab H Wahla, James H Tanner, James P Finn, Jamie S Mathews, Janete F Guardia, Janis S Gallagher, Jason D Tenney, Jay M Patria, Jeffrey J Thibodeau, Jeffrey S Buckser, Jessica D Spellman, Jessica I Newman, John A Hamilton, III, John A Hollings, John A Sciacchitano, John L Zaccone, John P Shelton, John R Carlson, Jonathan B Lewis, Jonathan G Matrisciano, Joppie, Joseph B Cascio, Joseph Foley, Joseph S Matrisciano, Joyce A Kellett, Joyce A Williams, Justine M Corson, Karen Mcnabb Noon, Katarzyna Plona, Kathleen A Sousa, Kathleen E Mcafoose, Kathleen M Curry, Kent A Conforti, Kristy B Yeaw, Lauren M Mclaughlin, Laurie B Frazier, LCDR Debra Emerson, Leo B Zadecky, Liz M Otero, Lorayne A Mcguinness, Louis Christy, Lyndsay M Perryman, Lynne M Dwyer, Marcia M Laughrey, Margaret E Walsh, Mark E Farrell, Martin J Guardia, Mary Jeanet Mcgarry, Maryam Tabatabaie, Maura Rooney, Mclaughlin, Megan A Haggerty, Michael E Antaya, Michael G Mayfield, Michael J Pasternak, Michael P Sweeney, Michelle M Noe Varga, Morgan J Matthews, Mutahar S Shamsi, Nabil Nakhoul, Nasser Yazdani, DVM, MPH, Nicholas J Scire, Nichole B Murphy, Oganr, Osama A Khatib, Pamela L Lee, Pamela L Ogonowski, Paraluman S Leonin, Paul P Geraci, Philip H Lafleur, Philip Kreiter, Ramcharan S Khalsa, Ramon E Martinez, Rebecca A Coleman, Remal, Richard F Hapke, Richard H Penta, Richard L Friedman, Richard L Licari, Richard W Skodinski, Robert D Ogan, Robert E Teel, Robert J Martin, Robert O'brian, Rory K Geyer, Rupa Pradhan, Sandra P White, Sara M Onyango, Sarah Forney, Sean M Tessicini, Seth A Mailhot, Shawn M Bogdan, Slater K Bartlett, Stacey S Degarmo, Stefan Kaszycki, Stephen C Smith, Steven M Ferrara, Sunita Pandey, Susan M Jackson, Suwaskie S Smith, Suzanne M Healy, Tamara S Rosbury, Teddy Tom, Terry C Kimball, Thomas Cote, Thomas J Kelly, Thomas J Murphy, Thomas O Morgan, Thomas Siebertz, Thomas W Nerney, Timothy M Glod, Torrance J Slayton, Troy R Petrillo, Vantwuyverc, Victoria Taylor, Wendy A Johnecheck, William K Dagley, Zhichao Lin, Zhong Y Wu

Lauren M Lawrance's Documents

Publish Date Document Type Title
November, 2012 FDA 483 Ameridose, LLC - Form 483, 2012-11-09
October, 2008 FDA 483 Blackstone Medical Inc. - Form 483, 2008-10-07
September, 2012 FDA 483 Brain Research, Inc. - Form 483, 2012-09-07
October, 2008 FDA 483 Response Blackstone Medical Inc. - Form 483R, 2008-10-31

Experience Redica Systems’ NEW investigator profiles and dashboards

Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:

  • Total inspections conducted
  • 483 rate
  • OAI rate
  • Warning Letter rate
  • Inspections by Industry, Scope, and Inspection Reason
  • And much more

Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.

FDA Investigator Profile Icon

Talk to sales to access our investigator profiles

Loading...

Investigator Profiles Are Just the Tip of the Iceberg

Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, but also grants you access to:

Inspection Intelligence

  • Pre-Approval Inspection (PAI) trends
  • The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
  • Latest 483s: see what the trends are across all FDA Investigators
  • CFR Heatmap: Citations aggregated by Subpart by Year

Vendor Intelligence

  • Full inspection histories for your vendors down to the specific site level
  • All of the functionality mentioned above but isolated to just your vendors

Regulatory Intelligence

  • Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
  • All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more