FDAnews Announces — Preparing for Global Track & Trace Regulations:Unbiased, Real-World Solutions Vendors Don’t Want You to Know Webinar, June 23, 2014

Over the next 10 years, more than 150 countries worldwide will require pharma track and trace regulations. Join FDAnews and track and trace expert Bill Fletcher of Pharma Logic Solutions on June 23, 2014 to tackle the numerous issues and misconceptions surrounding new track and trace requirements.

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FDAnews

FDAnews

Falls Church, VA (PRWEB) June 16, 2014

Preparing for Global Track & Trace Regulations:
Unbiased, Real-World Solutions Vendors Don’t Want You to Know
**FDAnews Webinar**
June 23, 2014 — 1:30 p.m. – 3:00 p.m. EDT
http://www.fdanews.com/GlobalTrack&Trace

Over the next 10 years, more than 150 countries worldwide will require pharma track and trace regulations.

Join FDAnews and track and trace expert Bill Fletcher of Pharma Logic Solutions on June 23, 2014 to tackle the numerous issues and misconceptions surrounding new track and trace requirements .

Mr. Fletcher has the kind of experience drugmakers really want to tap into. He's implemented 23 track and trace solutions internationally and is currently working on implementations 24 and 25.

He’s done them successfully and independently. Mr. Fletcher’s not affiliated with any hardware or software company; he's vendor agnostic.

His philosophy is this: With careful planning, drugmakers should only have to design their track and trace system once to successfully comply with current and future global regulations. They shouldn't have to incur additional expenses when other countries announce their versions of the regulation.

If a manufacturer is concerned about the new requirements for 150+ countries they won't want to miss out on this opportunity to get detailed input from this acknowledged expert. In just 90 minutes, attendees will:

  • Fully understand the track and trace requirements and why the FDA is enacting the policy
  • Get best practices for aligning the DSCSA requirements with requirements for other countries, including Brazil, China, European Union (EU) countries and more
  • Find out how to build a steering committee and expanded team that includes the proper subject matter experts
  • See what the GS1 (EPCIS, DPMS, GTIN, SSCC) standards really mean and how to use them to build one solution that will function successfully for all global regulations
  • Learn how to make use of the proven EDI 856 Transaction to speed development
  • Discover best practices for integrating serialization within existing SOPs — saving valuable training time and resources
  • Hear the dozens of lessons Mr. Fletcher has learned from implementing serialization at 25 global life sciences companies

Developing a global track and trace solution is likely to be one of the most significant IT and strategic challenges over the next 10 years. Drugmakers want to get it right the first time.

Make a small investment that will yield huge returns. Mark the calendar now for June 23, 2014, and attend Preparing for Global Track & Trace Regulations: Unbiased, Real-World Solutions Vendors Don’t Want You to Know.

Meet the Presenter:
William (“Bill”) Fletcher is the Managing Partner at Pharma Logic Solutions, LLC. His background spans over 32 years in pharmaceutical, supply chain software and healthcare systems, and he currently focuses on pharmaceutical serialization, track and trace and anti-counterfeiting for both commercial and clinical goods.

Who Will Benefit:

  • Drug companies
  • Biotech companies
  • Contract manufacturers
  • Wholesalers and distributors
  • 3PLs
  • Packaging companies

Webinar Details:
Preparing for Global Track & Trace Regulations:
Unbiased, Real-World Solutions Vendors Don’t Want You to Know
**FDAnews Webinar**
June 23, 2014 — 1:30 p.m. – 3:00 p.m. EDT
http://www.fdanews.com/GlobalTrack&Trace

Tuition:
$487 per site -- includes webinar registration and audio cds and transcripts

Easy Ways to Register:
Online: http://www.fdanews.com/GlobalTrack&Trace
By phone: 888-838-5578 or 703-538-7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.