FDA Investigator Christina J Sauder, PhD

Christina J Sauder, PhD has conducted inspections on 3 sites in 2 countries as of 06 Sep 2017. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:

Last Inspection Date:

06 Sep 2017

Investigator Role:

FDA Investigation Participant

Redica ID:

100003176

Countries of Inspections:

Canada, United States of America

FDA Investigators that have inspected at least one site in common with Christina J Sauder, PhD:

Alla Kachko, PhD, Anastasia I Offordile, Anissa M Cheung, Anita R Michael, Anita Verma, Ann L Demarco, Ann Marie Montemurro, Ann Marie Schofield, Audrey Thereset Uy, Brentley S Collins, Brian S Keefer, Burnell M Henry, CDR Jeremy L Wally, PhD, Chao Ming Tsai, Christian D Lynch (CDL), Christopher J Adams, Craig D Zagata, Cynthia Jim, CSO, Dave Hafner, David J Hafner, Debra J Bennett, Debra L Pagano, Diana Kouiavskaia, Donald L Lech, Eileen A Liu, Ellen Huang, Eric Peng, Gene D Arcy, Hala L Selby, Haruhiko Murata, Helen B Ricalde, J David Doleski, Jacqueline Mdiaz Albertini, James E Keller, PhD, James M Mason, James R Evans, Jennifer L Bridgewater, Joan A Loreng, Joan Adamo, Joan Johnson, Joanne M Hajoway, Joseph George, Julianne C Mccullough, Julie D Bringger, Junho Pak, Karyn M Campbell, Kathleen B Mihalik, Kathryn Carbone, MD, Kelly N Kerr, Kenneth M Gordon, Kristen D Evans, LCDR Margaret Edi Gennaro, Leslie D Wagner, Linda Thai, Lisa M Bellows, Lisa M Feola, LT John M Mastalski, Marian E Major, PhD, Michael Curbarg, Michael Gurbarg, Michele L Forster, PhD, Mihaly S Ligmond, Nancy T Waites, Omotunde O Osunsanmi, Paul W Keller, Paula A Trost, Prabhu P Raju, Ramon E Martinez, Rebecca K Olin, Robert B Shibuya, MD, Robert D Tollefsen, Roger F Zabinski, Ronald E Lundquist, Rose Ashley, Scott E Norris, Sheila Dreher Lesnick, Shuang Tang, Simone E Pitts, Stephanie Mangigian, MS/OSH, RN, Stephen D Brown, Steven A Rubin, Steven C Derrick, Susan F Laska, MS, Susan M Jackson, Tammy L Chavis, Tina Buecklein, Tina S Roecklein, Vlada Matusovsky, Wei Wang, PhD, Xiao Wang

Christina J Sauder, PhD's Documents

Publish Date	Document Type	Title
September, 2013	FDA 483	Sanofi Pasteur Limited - Form 483, 2013-09-20
September, 2013	FDA 483 Response	Sanofi Pasteur Limited - Form 483R, 2013-10-11
September, 2017	FDA 483	Sanofi Pasteur Limited - Form 483, 2017-09-22
February, 2013	FDA 483	Merck Sharp & Dohme LLC - Form 483, 2013-02-06

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.

Talk to sales to access our investigator profiles

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