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
  • SKIP TO CONTENT
  • SKIP NAVIGATION
  • Drug News
    • Trending
    • Commercial Operations
    • GMPs
    • FDA Enforcement Actions
    • Inspections and Audits
    • Postmarket Safety
    • Quality
    • Regulatory Affairs
    • Research and Development
    • Submissions and Approvals
    • FDAnews Drug Weekly
    • FDAnews
  • Device News
    • Trending
    • Commercial Operations
    • FDA Enforcement Actions
    • Inspections and Audits
    • Postmarket Safety
    • Quality
    • Regulatory Affairs
    • Research and Development
    • Submissions and Approvals
    • FDAnews Device Weekly
    • FDAnews
  • Books
    • FDAnews Books Library
    • Drug Books
    • Device Books
  • Training/Events
    • Webinar Training Pass
    • Events
  • Resources
    • Form 483s Database
    • FDA Approved Drugs
    • White Papers
  • CenterWatch
  • About Us
    • The Company
    • FDAnews Editorial Board
    • Contact Us
  • Advertising
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Authors » Marijo B. Kambere

Marijo B. Kambere

Products

PRODUCTS

Yibin Lihao Bio-technical Co., Ltd.

Marijo B. Kambere
$117.00
View

Hisun Pharmaceutical (Hangzhou) Co., Ltd.

Marijo B. Kambere
$117.00
View

Enantiotech Co., Ltd.

Marijo B. Kambere
$117.00
View

OXARC, Inc.

Marijo B. Kambere
$117.00
View

Abbott AMO (Hangzhou) Co., Ltd.

Peter E. Baker and Marijo B. Kambere
$117.00
View

Chongqing Pharmaceutical Research Institute Co., Ltd.

Peter E. Baker and Marijo B. Kambere
$117.00
View

Option Care Enterprises, Inc.

Gerard De Leon, Marijo B. Kambere, and Sangeeta M. Khurana
$117.00
View

Bend Research, Inc.

Christopher Czajka, Marijo B. Kambere, George Lunn, Anita Narula, and Robert D. Tollefsen
$117.00
View

Kirkman Laboratories, Inc.

Marijo B. Kambere and Marie P. Kelly-Doggett
$117.00
View

Upcoming Events

  • 28Sep

    The Cost of Counterfeiting: Why You Need a Plan to Secure Your Medical Device Supply Chain

  • 28Sep

    Calculating Sample Size to Satisfy FDA Expectations

  • 11Oct

    GMP Quality Management vSummit 2023: Where Quality Meets Risk

  • 16Oct

    MAGI@home Clinical Research Conference 2023

  • 26Oct

    FDA in 2024: What to Expect in an Election Year

  • 08Nov

    18th Annual FDA Inspections vSummit

Featured Products

  • FDA, FTC and DOJ Enforcement of Medical Device Regulations

    FDA, FTC and DOJ Enforcement of Medical Device Regulations

  • Using Real-World Evidence in Drug and Device Submissions

    Using Real-World Evidence in Drug and Device Submissions

Featured Stories

  • Manufacturing Cost is Key Issue Facing Gene Therapy Products, Marks Says

  • Artificial Womb Technology Not Yet Ready for Human Trials Adcomm Says

  • Top Concern for CBER is Marketing of Unapproved Biologics, Says FDA Official

  • FDA Deems Medline Industries’ Saline Solution Vial Recall as Class 1

The Revised ICH E8: A Guide to New Clinical Trial Requirements

Learn More
  • Drug Products
    • Quality
    • Regulatory Affairs
    • GMPs
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Device Products
    • Quality
    • Regulatory Affairs
    • QSR
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Clinical Products
    • Trial Design
    • Data Integrity
    • GCP
    • Inspections and Audits
    • Transparency
  • Privacy Policy
  • Do Not Sell or Share My Data
Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 703.538.7600 – Toll free 888.838.5578

Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing