FDA Investigator Martha T Olone

Martha T Olone has conducted inspections on 11 sites in 3 countries as of 10 Jan 2012. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
11
Last Inspection Date:
10 Jan 2012
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
Canada, United States of America, Austria
FDA Investigators that have inspected at least one site in common with Martha T Olone:
Aimee Cunningham, PhD, Alicia M Mozzachio, Althea A Williams, Amanda Dinaro, Amanda S Zorn, Amber D Brodas, Amy Devlin, PhD, Amy M Cramer, Ana S Cabrera, Anissa M Cheung, Ann Marie Montemurro, Ann Marie Schofield, Anna Flynn, Annemarie Bodnar, Antonina Aydanian, Arie C Menachem, Atul J Agrawal, Azza Talaat, Brenda P King, Brentley S Collins, Brian D Nicholson, Bruce H Mccullough, Burnell M Henry, Byungja E Marciante, Carolyn A Renshaw, Carrie Ann Plucinski, Cassandra Overking, CDR Jeremy L Wally, PhD, Chad E Schmear, Chad R Burger, Charles Jewell, Chiang Syin, PhD, Christian D Lynch (CDL), Christina Capacci Daniel, PhD, Christopher Downey, PhD, Creighton T Tuzon, Cynthia Jim, CSO, Daniel C Kearns, Daniel Kearns, Dawn L Wydner, Dawn M Braswell, Deborah M Trout, Debra I Love, Debra Lboyd Seale, Demitria J Argiropoulos, Demitria J Xiradakis, Dennis E Guilfoyle, PhD, Diane L Raccasi, Dolores Harper, Donald L Lech, Dr. Guang Gao, PhD, Dr. Willie F Vann, PhD, Dr. Zhihao Qiu (Peter), PhD, Edward A Brunt, Ekaterina Allen, Eliezar Ramos, Ellen P Madigan, Elliot P Cowam, PhD, Eric J Cunningham, Eric M Mueller, PharmD, Esra Toussaint, Frank J Marciniak, Freyja V Lynn, Gene D Arcy, Gunther Boekhoudt, PhD, Helen B Ricalde, Humera T Khan, J David Doleski, Jacqueline Mdiaz Albertini, Jacqueline S Warner, James C Maclaughlin, James E Keller, PhD, James W Plucinski, Jan B Welch, Janet L Bowen, Jason F Chancey, Jean M Kelahan, Jeanne M Morris, Jee Chung, PhD, Jennifer L Bridgewater, Jennifer L Schmidt, Jennifer Macmillan, Jesse A Vazquez, Joan A Loreng, Joanne Pryzbylik, Jonathan G Matrisciano, Jose R Hernandez, Joseph A Morkunas, Joyce A Rockwell, Julie D Bringger, Justine M Corson, Kara A Scheibner, PhD, Karen Emasley Joseph, Karen L Kosar, Kathleen B Swat, Kathleen R Jones, PhD, Kelly I Anderson, Kevin A Gonzalez, Kimberly Lewandowski Walker, Kimberly M Bigler, Kinh Q Mac, Kristina L Conroy, Kujtim Sadiku, Lakisha M Williams, Lata C Mathew, PhD, Lauren L Vajo, Laurie A Haxel, LCDR Debra Emerson, Lequita M Mayhew, Leslie D Wagner, Li Li, Linda Thai, Lindsey R Lyman, Lisa Hornback, Lorelei S Jarrell, Loretta Nemchik, Lori Peters, Margaret Torres Vazquez, Maria Joselopez Barragan, PhD, Marion Michaelis, Mariza M Jafary, Marjorie A Shapiro, PhD, Marsha W Major, Martha O'lone, Mary Davis Lopez, Mary T Carden, Mate Tolnay, Matthew A Spataro, Maureen C Melvin, Maxwell Van Tassell, PhD, Megan A Haggerty, Meihong Liu, Michael D Robinson, Michael Schmitt, Michele L Forster, PhD, Michelle M Noe Varga, Mihaly S Ligmond, Mikhail V Ovanesov, PhD, Milan S Blake, Monique C Lo, Nailing Zhang, Nancy T Waites, Nicholas F Lyons, Nicole J Clausen, Nicole K Trudel, Nicole S Williams, Nisha C Patel, Norman Wong, Ogechi C Nna, Omotunde O Osunsanmi, Paul Mouris, Paula A Trost, Perry T Nichols, Prabhu P Raju, Priscilla M Pastrana, Qiao Y Bobo, Rafael Padilla, Richard D Manney, Richard H Penta, Richard T Riggie, Richard W Thornton, Robert J Martin, Robert Jennings, Robert L Stevenson, Roberta W Cunningham, Roger F Zabinski, Rose Ashley, Russell K Riley, Sarah B Tanksley, Sarah Forney, Scott E Norris, Sean R Marcsisin, Seth A Mailhot, Sheryl A Kochman, Simone E Pitts, Stacey S Degarmo, Stephen D Eich, Susan A Zullo, PhD, Susan F Laska, MS, Susan M Jackson, Susan Yu, Tamara Brey, Teresita C Mercado, Tina S Roecklein, Todd M Stankewicz, Travis S Bradley, Victor J Gangi, Walter N Lange, Wayne E Seifert, Yanming An, PhD, Yvins Dezan, Ze Peng

Martha T Olone's Documents

Publish Date Document Type Title
May, 2008 FDA 483 ID Biomedical - Form 483, 2008-05-22

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