Pharmaceutical Traceability

May 23-25, 2016 | Sheraton Downtown Hotel, Philadelphia, PA

Welcome back to our 3rd edition of the Pharmaceutical Traceability Forum. Your #1 industry resource for compliance with domestic and international pharmaceutical traceability regulations and guidelines…

With the global drug counterfeiting trade on the rise and regulatory deadlines fast approaching, the pharmaceutical supply chain finds itself at a critical point. Faced with stakes that are higher now than ever before, all trading partners in the supply chain, from drug manufacturers to distributors to dispensers, must act now and act fast in order to upgrade their production lines to comply with fast-approaching traceability deadlines, and more importantly, ensure maximum patient safety.

To add to these complexities, international country specific deadlines and compliance requirements are currently being updated. How can companies ensure strategy flexibility and update their present timelines and processes to account for new changes emerging out of countries such as Russia, Saudi Arabia, Korea, Brazil and Turkey? Both big and small pharma are doing their best to leverage their internal teams, establish quality vendor relationships, and budget accordingly for this enormous ongoing investment.

Here is where we can help!  IQPC’s 3rd Pharmaceutical Traceability Form has brought together industry thought leaders to walk you through the tedious process of serialization and provide invaluable insight into what is coming next in 2016 and beyond.  Gain an in-depth perspective on the ever-changing international regulations, data interoperability, and explore the cutting-edge FDA pilot programs in our dynamic workshops.  Take advantage of the opportunity to hear new innovated programs put in place by top companies in our unique case studies and walk away with a deep understanding of key industry trends and solutions.

Come the discussion with thought leaders from a range of expertise, including:

  • Supply chain management
  • Serialization
  • Track & trace
  • Anti-counterfeiting
  • Aggregation
  • Product Recalls
  • SAP/Aii OER
  • Validation engineering
  • Data interoperability
  • Master data
  • Packaging & Labeling operations
  • Brand protection
  • US and international regulations
  • Cargo theft
  • CMO/CPO on-boarding

...and so much more!

Featured Speakers

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Why Attend?

From startup and mid-size pharma to multi-national giants, we’ll address the challenges that are unique to manufacturers, distributors, dispensers, CMOs and CPOs according to varying sizes and resources. But we’ll also be tackling the tough questions that are common to all, such as

Interactive Sessions

Analyze

established pilots aimed to evaluate & improve existing methods for tracing serialized products throughout the supply chain while examining benefits of aggregation

Real Situation Analysis

Create

a brand protection culture within your organization to better secure your patients’ safety against counterfeiting

ISO Technical Committee

Streamline

you CMO/CPO integration to cut down on delays by creating common standards for serialized product event exchanges and data transfer

Reduce Costs and Improve Quality

Achieve

global harmonization by standardizing your operations across borders while remaining ahead of changing international deadlines

Networking Opportunities

Innovate

ways to use this vast collection of serialized data to serve your end-user in pursuit of enhanced returns

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