Question
As originally asked by
Louis Coenders
Experienced interim professional for European freight, warehousing & logistics assignments | Europe - NL - Venlo |
June 2016
Hi, I need your help. I would really appreciate to learn what channels/methods are suitable to make medical device manufacturers and distributors aware on European logistics and warehousing services for Medtech devices. Tradeshows like Medica, Arab H...
During the 10x conference in San Diego last month, we discussed the changes to the EU regulations for CE Marking. If you are interested in downloading the slide decks for free, please visit the following link:http://medicaldeviceacademy.com/10x-2016/...
Veteran device CEO Joseph Gulfo says, "The FDA must be challenged (when appropriate) because it operates in a highly political environment and has strayed from its original mandate." His full 2016 10x Medical Device Conference talk, slides, and trans...
JoAnne Moody
Adhesive Consultant ► Solving Adhesive, Coatings, & Plastic Problems ► Moving Your Project Forward ► Medical Devices
May 2016
An amazing advancement in cancer treatment ( https://www.youtube.com/watch?v=Pxy8K58VYvA ) Learn from Steve Mohr, Senior Engineer, Varian Medical Systems, speaking at Conference on June 9, Santa Clara, CA ( http://smesv.org/conference ) 20+ speakers....
Is it mandatory to have GS1 GTIN barcoding on medical device? I understand US FDA has made UDI mandatory, but for a company which is not targeting US market is it good to have a GS1 GTIN barcoding in place. source: https://www.linkedin.com/groups/786...
In the traditional “Big Pharma” drug development model, a new drug is created to address a disease and, based on objective evidence, reviewed and labeled for treatment for a specific list of ailments (although a physician can Rx it for off label uses...
Recently some of my clients received 483 observations for supplier controls and MDR reporting, but one of my clients asked which areas are FDA inspectors emphasizing. I noticed no significant changes, but I thought it was worth revisiting my Pareto A...
Another great event by MassBio/MDG (Medical Development Group of Boston) this morning. A cautionary point made: Don't use "full service" design and development firms unless you know they have core competencies in the area you need. Be sure the organi...
Our fourth 10x Medical Device Conference was a great success in part from presentations like the one I'm sharing with you today. Mid-market M&A specialist Deborah Douglas told us how to determine when it's time to sell your medical device company. Fu...
