Gary Saner's guest appearances

Gary Saner

Global Medical Device Podcast powered by Greenlight Guru

Business Growth Café

Dave Daley

Bryan Thompson

Scott Miller

Meghan Alonso

Leo Eisner

Mike Drues

Peter Sebelius

Steve Hoffman

Jack Kelly

Michael Carroll

Steve Pitchford

Matt Everitt

Patrick Schwerdtfeger

Michael Drues

Ronny Bracken

OwlTail

What does it take to take an idea and grow it into a business with multiple employees, serving clients in a wide variety of industries in a very competitive market? CEO Gary Saner of software developer Primero Systems joined us to share insights that will benefit any business in its efforts to build an enduring brand.

What does it take to take an idea and grow it into a business with multiple employees, serving clients in a wide variety of industries in a very competitive market? CEO Gary Saner of software developer Primero Systems joined us to share insights that will benefit any business in its efforts to build an enduring brand.

Software's Limitless Capabilities! With Gary Saner, CEO of Primero Systems

If you are part of an organization developing or producing Class II medical devices, you should know that on September 24, 2016, your UDI submissions are due to the FDA.“I don’t mean to scare anyone, but we only have 78 working days left.” - Gary SanerUDI stands for “unique device identification,” and the new labeling regulations have been put into place to increase patient safety, reduce medical errors, and provide a foundation for secure global distribution of devices.Today’s guest, Gary Saner, is an expert on UDI submissions and other regulatory topics. As the Senior Manager of Information Solution at Reed Tech, Gary is speaking to us today about the UDI submission procedures and other relevant topics.“The UDI submission is not a one-time effort.” - Gary SanerWith over 30 years’ experience in software management and data conversion, Gary is the go-to person if you have questions about UDI, and his company can help medical device companies of any size be sure that their submissions are in order. Some of the topics you’ll hear discussed on today’s podcast include:- What UDI is and what information needs to be included in each of its components.- The timeline of deadlines leading up to now and up to September 2016 as they pertain to different types of devices.- Some of the challenges that apply to larger and smaller companies when it comes to meeting the 9/24/16 deadline, as well as how the Reed Tech tool can help organizations of all sizes.- The importance of knowing and understanding the UDI submission process.- The two submission methods that the FDA has in place.- Tips and pointers to keep in mind as you go through the submission process.

If you are part of an organization developing or producing Class II medical devices, you should know that on September 24, 2016, your UDI submissions are due to the FDA. “I don’t mean to scare anyone, but we only have 78 working days left.” - Gary Saner UDI stands for “unique device identification,” and the new labeling regulations have been put into place to increase patient safety, reduce medical errors, and provide a foundation for secure global distribution of devices. Today’s guest, Gary Saner, is an expert on UDI submissions and other regulatory topics. As the Senior Manager of Information Solution at Reed Tech, Gary is speaking to us today about the UDI submission procedures and other relevant topics. “The UDI submission is not a one-time effort.” - Gary Saner With over 30 years’ experience in software management and data conversion, Gary is the go-to person if you have questions about UDI, and his company can help medical device companies of any size be sure that their submissions are in order. Some of the topics you’ll hear discussed on today’s podcast include: - What UDI is and what information needs to be included in each of its components. - The timeline of deadlines leading up to now and up to September 2016 as they pertain to different types of devices. - Some of the challenges that apply to larger and smaller companies when it comes to meeting the 9/24/16 deadline, as well as how the Reed Tech tool can help organizations of all sizes. - The importance of knowing and understanding the UDI submission process. - The two submission methods that the FDA has in place. - Tips and pointers to keep in mind as you go through the submission process.

Preparing Your Class II Device for the UDI Compliance Deadline with Gary Saner