FDA Investigator Julie Rorberg
Julie Rorberg has inspections in 1 countries as of 23 Feb 2022. Julie Rorberg has collaborated with a combined 557 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
3
Last Inspection Date:
23 Feb 2022
Investigator Role:
FDA Investigation Participant
Redica ID:
Country:
United States of America
Co-Investigator(s):
Amalia C Himaya,
Arsen Karapetyan,
Babajide Michael Osunsanmi,
Benjamin S Liao,
Binh T Nguyen,
Brian J Ryan,
Brien C Fox,
Bryan A Galvez,
Carla J Lundi,
Carr Sharpe,
Caryn M Everly,
Caryn M Mcnab,
Chelsea N Sealey,
Julie A Rorberg,
Julie A Stocklin,
Kelley,
Ling Yul Liu,
Michael D Garcia,
Nicholas L Hunt,
Richard C Chiang,
Rumany C Penn, PharmD,
Saied A Asbagh,
Selene T Torres,
Stephanie A Slater, MS,
Tamala P Magee,
Terri L Dodds,
Thomas J Arista,
Uttaniti Limchumroon (Tom),
Vickie L Anderson,
Virgilio F Pacio, CSO,
Yvonne T Lacour,
Zachary A Bogorad
Julie Rorberg's Documents
Publish Date | Document Type | Title |
---|---|---|
October, 2000 | EIR | MD Pharmaceuticals aka Celltech Manufacturing - EIR, 2000-10-24 |
November, 2001 | FDA 483 | Bachem Americas, Inc. - Form 483, 2001-11-27 |
October, 2000 | FDA 483 | MD Pharmaceuticals aka Celltech Manufacturing - Form 483, 2000-10-24 |
November, 2001 | EIR | Bachem Americas, Inc. - EIR, 2001-11-27 |
June, 2001 | EIR | Bachem Americas, Inc. - EIR, 2001-06-08 |
November, 2001 | FDA 483 Response | Bachem Americas, Inc. - Form 483R, 2001-11-27 |
June, 2001 | FDA 483 | Bachem Americas, Inc. - Form 483, 2001-06-08 |
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](https://redica.com/document-store/images/InspectorProfile.png)
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