We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our
Cookie Policy
.
Accept
Label
Search
SKIP TO CONTENT
SKIP NAVIGATION
Drug & Device Products
FDAnews Books Library
Events
Form 483s Database
Publications
Webinar Training Pass
eCFR and Guidances
Books
Clinical Products
Advertising
White Papers
Contact Us
About Us
COVID-19
Sign In
Create Account
Sign Out
My Account
Home
»
Authors
» Michele L. Obert
Michele L. Obert
Products
PRODUCTS
Dong Yuan Technology Co., Ltd.
Michele L. Obert
Price:
$117.00
View
Jiangxi Long Life Bio-Pharmaceutical Co., Ltd.
Michele L. Obert
Price:
$117.00
View
AML Riverside, LLC
Wayne D. McGrath
and
Michele L. Obert
Price:
$117.00
View
Surmasis Pharmaceutical
Brett R. Havranek
and
Michele L. Obert
Price:
$117.00
View
American Laboratories, Inc.
Diana K. Krepel
and
Michele L. Obert
Price:
$117.00
View
American Laboratories, Inc.
Diana K. Krepel
and
Michele L. Obert
Price:
$117.00
View
Essential Isotopes LLC
Michele L. Obert
Price:
$117.00
View
Meridian Medical Technologies, Inc.
Zedong Dong
,
Rick L. Friedman
,
Kellia N. Hicks
,
John C. McMichael
,
Michele L. Obert
,
Phillip M. Pontikos
, and
Frank Wackes
Price:
$117.00
View
Triad Isotopes, Inc.
Michele L. Obert
Price:
$117.00
View
Bayer Health Care, LLC
Michele L. Obert
Price:
$117.00
View
View All Products by Michele L. Obert
Upcoming Events
08
Sep
Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections
15
Sep
Califf’s Post-PDUFA, Post-COVID FDA Agenda: Key Developments, Insights and Analysis
20
Sep
Building a World-Class Pharmaceutical Advertising and Promotion Review Program
21
Sep
The FDA’s Focus on Clinical Data Integrity Throughout Product Development and Approval
22
Sep
FDA’s New Quality Management System Regulation: What the Proposed Harmonization with ISO 13485 Means for Devicemakers
11
Oct
1st Annual Quality Management vSummit
Featured Products
FDA’s New Quality System Regulation: Transitioning from QSR to ISO 13485
Selecting and Implementing Electronic Document Management Systems in the EU
Featured Stories
Thermo Fisher Scientific Gets FDA Premarket Approval for Companion Diagnostic
MHRA Grants Conditional Authorization to Moderna’s Bivalent COVID-19 Booster Vaccine
Organogenesis Gets 510(k) Clearance to Expand PuraPly Portfolio
FDA Grants Priority Review to sNDA for Lynparza
The Revised ICH E8:
A Guide to New Clinical Trial Requirements
Learn More
