Mark Jackson
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Medical Device Conference 2011, Anaheim California
Schedule
Each session runs all day, from 9 am – 4:00 pm
Here is just a sample of some of the great programs. I signed up for the ones in red. Last year, only myself, the guys from NADX, DSG and Glidewell were there representing labs. Most of the big dental manufacturers were there.
Monday, February 7
#100 FDA 510(k) Update. Everything you need to know about the FDA 510k process and how products come to market, how you can use them...and how you SHOULD NOT use them.
#101 Establishing and Maintaining a Total Quality Management System
Establishing FDA GMP guidelines in your laboratory, and how to be FDA compliant.
#102 Applied Innovation The benefits of quick and rough prototyping.
#103 Materials Selection and Compatibility Biomaterials update, with a focus in implantable devices.#104 Quality Engineering: A Lifecycle Approach Business drivers and Business Defenders. FDA
Tuesday, February 8
#200 Surviving a New Era of FDA Enforcement
#201 Working with FDA
#202 Product Development and FDA Approval Process for Medical Devices
#203 Materials for Implants and other Demanding Biomedical Applications
#204 Medical Device Packaging Update
Wednesday, February 9
#300 Surviving a New Era of FDA Enforcement, cont
#301 Process Validation: Solutions and Strategies for the Medical Device Industry
#302 Design for Manufacture and Assembly of a Medical Device
#303 Working with Modern Materials
#304 Strategies to Engage a Diverse Supply Chain
Thursday, February 10
#400 FDA/Industry Communication: Resolving Issues and Avoiding Problems
#401 Advanced Process Validation
#402 Current Events and Trends in Software Validation
# 403 Developing Resorbable Implants: an industry Perspective
#404 Risk Management for Medical Devices: Applying 14971 Effectively Using Risk Assessment and Reliability Tools
Schedule
Each session runs all day, from 9 am – 4:00 pm
Here is just a sample of some of the great programs. I signed up for the ones in red. Last year, only myself, the guys from NADX, DSG and Glidewell were there representing labs. Most of the big dental manufacturers were there.
Monday, February 7
#100 FDA 510(k) Update. Everything you need to know about the FDA 510k process and how products come to market, how you can use them...and how you SHOULD NOT use them.
#101 Establishing and Maintaining a Total Quality Management System
Establishing FDA GMP guidelines in your laboratory, and how to be FDA compliant.
#102 Applied Innovation The benefits of quick and rough prototyping.
#103 Materials Selection and Compatibility Biomaterials update, with a focus in implantable devices.#104 Quality Engineering: A Lifecycle Approach Business drivers and Business Defenders. FDA
Tuesday, February 8
#200 Surviving a New Era of FDA Enforcement
#201 Working with FDA
#202 Product Development and FDA Approval Process for Medical Devices
#203 Materials for Implants and other Demanding Biomedical Applications
#204 Medical Device Packaging Update
Wednesday, February 9
#300 Surviving a New Era of FDA Enforcement, cont
#301 Process Validation: Solutions and Strategies for the Medical Device Industry
#302 Design for Manufacture and Assembly of a Medical Device
#303 Working with Modern Materials
#304 Strategies to Engage a Diverse Supply Chain
Thursday, February 10
#400 FDA/Industry Communication: Resolving Issues and Avoiding Problems
#401 Advanced Process Validation
#402 Current Events and Trends in Software Validation
# 403 Developing Resorbable Implants: an industry Perspective
#404 Risk Management for Medical Devices: Applying 14971 Effectively Using Risk Assessment and Reliability Tools
