June 6-8, 2011 | Bethesda North Marriott Hotel | Bethesda, Maryland
Conference 6-7 | Exhibition 6-7 | Course 8
Register by May 5th and save up to $200!
At the 2011 PDA/FDA Pharmaceutical Supply Chain Conference & TRI Course, US and EU regulators along with industry experts will discuss the current threats of today's supply chain and present innovative approaches aimed at preventing illicit acts such as counterfeiting, diversion, and economic adulteration.
As supply chain security continues to evolve into a global initiative, as well as a cross-departmental initiative, global regulators must partner, just as industry must partner to promote patient safety. To support these collaborative efforts, this year's program agenda will cover the entire supply chain, from end-to-end; with one track focused on materials security and the other focused on finished product security.
Sessions topics include:
• Supply Chain Security-A Global Initiative
• Risk Model: Materials
• Risk Model: Finish Products
• Supply Channel Tracking: Materials
• Supply Channel Tracking: Finish Products
• Solutions that you Can Use Today
• Creating the End-to End Approach
• 3rd Party Audit Solutions
• Security of Materials
• Ensuring Secure Distribution of Finished Product
• The Threats are Real: We Must Remain Steadfast in Our Mission to Protect Patients
• And more! - view the full agenda!
New! An audience response system will be used to engage all participants during each plenary session. This will provide a unique speaker and audience interaction as well as real-time benchmarking information.
Don't allow a public health crisis due to an incident in the supply chain to happen. Plan to attend the 2011 PDA/FDA Pharmaceutical Supply Chain Conference & TRI Course and help us forge the types of changes that can promote the security of our drug supply.
Register now!
Following the conference, participants can develop additional knowledge about Developing a Robust Supplier Management Process at the stand-alone course hosted by the PDA Training and Research Institute (PDA TRI) on June 8th.
Conference 6-7 | Exhibition 6-7 | Course 8
Register by May 5th and save up to $200!
At the 2011 PDA/FDA Pharmaceutical Supply Chain Conference & TRI Course, US and EU regulators along with industry experts will discuss the current threats of today's supply chain and present innovative approaches aimed at preventing illicit acts such as counterfeiting, diversion, and economic adulteration.
As supply chain security continues to evolve into a global initiative, as well as a cross-departmental initiative, global regulators must partner, just as industry must partner to promote patient safety. To support these collaborative efforts, this year's program agenda will cover the entire supply chain, from end-to-end; with one track focused on materials security and the other focused on finished product security.
Sessions topics include:
• Supply Chain Security-A Global Initiative
• Risk Model: Materials
• Risk Model: Finish Products
• Supply Channel Tracking: Materials
• Supply Channel Tracking: Finish Products
• Solutions that you Can Use Today
• Creating the End-to End Approach
• 3rd Party Audit Solutions
• Security of Materials
• Ensuring Secure Distribution of Finished Product
• The Threats are Real: We Must Remain Steadfast in Our Mission to Protect Patients
• And more! - view the full agenda!
New! An audience response system will be used to engage all participants during each plenary session. This will provide a unique speaker and audience interaction as well as real-time benchmarking information.
Don't allow a public health crisis due to an incident in the supply chain to happen. Plan to attend the 2011 PDA/FDA Pharmaceutical Supply Chain Conference & TRI Course and help us forge the types of changes that can promote the security of our drug supply.
Register now!
Following the conference, participants can develop additional knowledge about Developing a Robust Supplier Management Process at the stand-alone course hosted by the PDA Training and Research Institute (PDA TRI) on June 8th.
