FDA Investigator Xianghong Jing (Emily), PhD
Xianghong Jing (Emily), PhD has conducted inspections on 4 sites in 4 countries as of 09 Dec 2021. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
4
Last Inspection Date:
09 Dec 2021
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America,
Switzerland,
Austria,
Denmark
FDA Investigators that have inspected at least one site in common with Xianghong Jing (Emily), PhD:
Anissa M Cheung,
Anita Narula, PhD,
Anthony F Lorenzo,
Arsen Karapetyan,
Barbara Janine Breithaupt,
Bo Chi, PhD,
Brandon C Heitmeier,
Brian M Janelsins, PhD,
Bruce H Mccullough,
CDR Cecily Jones,
CDR Jeremy L Wally, PhD,
Chikako Torigoe, PhD,
Christian D Lynch (CDL),
Christopher Downey, PhD,
Craig A Garmendia,
David G Eng,
Deborah Schmiel, PhD,
Dennis Cantellops Paite,
Douglas A Campbell,
Dr. Ralph M Bernstein, PhD,
Edmund F Mrak, Jr,
Ephrem Hunde, PhD,
Gene D Arcy,
George Pyramides,
Gloria E Parra,
Gwyn G Dickinson,
Haruhiko Murata,
Holly Brevig,
Jacek Cieslak, PhD,
Jacqueline Mdiaz Albertini,
James D Bridges,
James I Giefer,
James L Dunnie, Jr,
Jean Lhu Primmer,
Jose A Lopez,
Jose Acruz Gonzalez,
Kalavati Suvarna, PhD,
Kevin A Gonzalez,
Kevin D Kallander,
Kevin P Foley,
Larry K Austin,
Lawrence J Stringer,
Margaret M Annes,
Maria Gutierrez Lugo, PhD,
Maria Joselopez Barragan, PhD,
Melissa D Ray,
Michael A Charles,
Michael E Maselli,
Michael J Vardon,
Michael Shanks, MS,
Michelle Yclark Stuart,
Mra V Millarw,
Niketa Patel,
Pankaj H Amin,
Parul M Patel,
Patricia F Hughes, PhD,
Patrick L Wisor,
Patsy J Domingo,
Paul A Bonneau,
Paul W Keller,
Penny H Mccarver,
Prabhu P Raju,
Priscilla M Pastrana,
Randa Melhem, PhD,
Rashmi Rawat, PhD,
Rebecca E Dombrowski,
Rebecca Rodriguez,
Reyes Candau Chacon, PhD,
Robert D Tollefsen,
Samina S Khan,
Santos E Camara,
Sidney B Priesmeyer,
Simone E Pitts,
Stephen D Eich,
Steven A Rubin,
Susan M Jackson,
Susan T Hadman,
Tawny L Colling,
Thomas J Arista,
Thuy T Nguyen, LCDR,
Tina M Pawlowski,
Torrance J Slayton,
Wayne E Seifert,
Xiao Wang,
Yehualashet A Gessesse,
Zhong Li, PhD
Xianghong Jing (Emily), PhD's Documents
Publish Date | Document Type | Title |
---|---|---|
December, 2021 | FDA 483 | Sandoz GmbH - Form 483, 2021-12-17 |
July, 2016 | FDA 483 | FUJIFILM Diosynth Biotechnologies Denmark ApS - Form 483, 2016-07-08 |
January, 2016 | FDA 483 | F. Hoffmann-La Roche AG - Form 483, 2016-01-22 |
February, 2014 | FDA 483 | Seqirus Inc - Form 483, 2014-02-12 |
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
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