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.
  • SKIP TO CONTENT
  • SKIP NAVIGATION
  • Drug Products
    • Books
    • FDAnews Books Library
    • Events
    • Form 483s Database
    • Subscription Newsletters
    • Free Newsletters
    • Webinar Training Pass
    • eCFR and Guidances
  • Device Products
    • Books
    • FDAnews Books Library
    • Events
    • Form 483s Database
    • Subscription Newsletters
    • Free Newsletters
    • Webinar Training Pass
    • eCFR and Guidances
  • Clinical Products
  • Advertising
  • White Papers
  • Contact Us
  • About Us
  • COVID-19
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Drug Development Meetings

Drug Development Meetings

May 4, 2006

Join FDAnews Thursday, May 18, for a 90-minute audioconference, "Designing Pregnancy Registries: Strategies to Ensure Maximum Retention and Data Collection" Monica Kumar, associate medical director for Covance, will reveal the common pitfalls that could jeopardize your pregnancy registry, and how to prevent them. On May 24, join FDAnews for "Clinical Trial Billing Under Medicare: Negotiate Trial Budgets to Steer Clear of the OIG." In this 90-minute audioconference with Q&A session, noted attorney Mark Barnes will show you how to negotiate a clinical trial budget that keeps your sites operating and billing in compliance.

May 8-10: Generic Drug Approvals Amsterdam, the Netherlands 31 20 638 28 06 Center for Professional Advancement amsterdam@cfpa.com www.cfpa.com

May 9-10: How to Monitor Clinical Trials for GCP Compliance Dublin, Ireland

(610) 688-1708 The Center for Professional Innovation and Education info@cfpie.com

www.cfpie.com/showitem.aspx?productid=043&source=fdanewsconferencecalendarfree

May 11-12: Complying with the EU Clinical Trial Directive Morristown, NJ (212) 661-3250 PTi international dweinberg@pti-international.com www.pti-international.com

May 15-17: Non-clinical Drug Safety Evaluation & Drug Development Amsterdam, the Netherlands 31 20 638 28 06 Center for Professional Advancement amsterdam@cfpa.com

www.cfpa.com

May 21-24: Outsourcing & Offshoring Clinical Trials

Boston, Mass. (773) 695-9400 Advanced Learning Institute bob@aliconferences.com

www.aliconferences.com

May 22-23: Complying with the EU Clinical Trial Directive Washington, DC (212) 661-3250 PTi international dweinberg@pti-international.com

www.pti-international.com

May 22-24: Skin Product Development Amsterdam, the Netherlands 31 20 638 28 06 The Center for Professional Advancement

amsterdam@cfpa.com www.cfpa.com

May 24: Clinical Trial Billing Under Medicare Negotiate Trial Budgets to Steer Clear of the OIG An audioconference

Your Office (703) 538-7600 http://www.fdanews.com/wbi/conferences/ctbilling.html

May 25-26: Project Management in Drug Development: Phase I and Phase II Clinical Development

San Diego, Calif. (212) 661-3250 PTi international dweinberg@pti-international.com

www.pti-international.com

May 29-31: Microbiological Control & Validation Amsterdam, the Netherlands 31 20 638 28 06 The Center for Professional Advancement amsterdam@cfpa.com www.cfpa.com

May 31: Best Practices in Electronic Data Capture for Clinical Trials Tips to Cut Costs and Increase Efficiency An audioconference Your Office (703) 538-7600 http://www.fdanews.com/wbi/conferences/datacapture.html

June 1-2: Clinical Trials for Pharmaceuticals: Design and Development Boston, Mass. (610) 548-2200 Barnett Educational Services customer.service@parexel.com

www.barnettinternational.com/index-flash.html

KEYWORDS Drug Pipeline Alert

Upcoming Events

  • 10Mar

    FDA Drug GMP Facility Inspections During the Pandemic

  • 16Mar

    Pharmaceutical Naming Regulation: Understanding the Latest Developments

  • 18Mar

    Pharmaceutical Postmarket Surveillance: Latest Developments in the Era of COVID-19

  • 23Mar

    Data Integrity for GCP Professionals: Core Requirements, Expectations and Challenges

  • 30Mar

    Data Integrity for GMP/Postmarket Professionals: Core Requirements, Expectations and Challenges

  • 06Apr

    Medical Device Cybersecurity: Understand the Latest Developments

Featured Products

  • Biological Risk Evaluation and Management for Medical Devices

  • GMP Inspection Preparation Checklist: A Tool for Internal Auditing

Featured Stories

  • WhiteHouse.gif

    President Biden Issues Executive Order on U.S. Supply Chain

  • roche.gif

    Priority Healthcare Settles Diabetes Test Lawsuit with Roche for $43 Million

  • Effective text

    Pfizer/BioNTech Vaccine Equally Effective for All Age Groups, Israeli Study Says

  • Siemens Healthineers logo

    Siemens Healthineers’ COVID-19 Antigen Lab Test Receives CE Mark

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 My Personal Information
Footer Logo

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

Phone 703.538.7600 – Fax 703.538.7676 – Toll free 888.838.5578

Copyright © 2021. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing