San Francisco, California Area FDA Registered Finished Device Contract Manufacturers and Sterilizers

Sam Lazzara
Resume
LinkedIn Profile 
Documents
Services
Schedule Call 


+1 510 397 9739
sam@lazzara.net

Think global, buy local...and local for me is the San Francisco, California USA area.

Here is a link to a list I compiled for SF Bay Area FDA Registered Medical Device Contract Manufacturers and Sterilizers.

This list is focused on finished device manufacturers and contract sterilizers who are registered as such with FDA, and are located in the 9 counties in the SF Bay Area. 

As I update the list with new information I receive, the same link should still work.
The list has a footer with my contact info and the last revision date.

Any comments, questions or suggestions are very welcome.

There were a few firms recommended to me for the list that are not included since I was not able to verify FDA registration either via the FDA search or by directly contacting the firm.  Interestingly, not all firms who are FDA registered appear when you try to search for them here:
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm

Sam Lazzara
Resume
LinkedIn Profile 
Documents
Services
Schedule Call 


+1 510 397 9739
sam@lazzara.net

Popular posts from this blog

ISO 13485:2016 Quality System Process Risk Management

Image
I SO 13485:2016 has a broader view of risk management than in the past. Risks are to be considered in terms of the impact on medical device safety and performance, and in terms of meeting regulatory requirements. For managing quality system process risks, rather than adding a Risk section to each Standard Operating Procedure (SOP) as some have suggested, I added a new section to my Quality Manual to address risks for each quality system process, i.e. each SOP. The front end of my new Quality Manual risk section is shown below.  A row is included in the table for each SOP. Since my Quality Manual already lists the SOPs, this makes sense to me. And by having all of the risk assessment and control information in this single document, it seems easier to manage than sprinkling risk assessment/control info into each SOP.  Sam Lazzara Resume LinkedIn Profile Documents Services
Read more

Put ISO 13485:2016 in your rear-view mirror

Image
Enough is enough! You heard that ISO 13485:2016 was published in March 2016, and maybe you purchased the standard. But with everything else going on in your life, you have not had the time to figure out how or when to deal with it. Well....now is the time to get the 13485 monkey off your back. Starting from scratch? I have cracked the 13485:2016 nut, and can provide a full deck of documents tailored to your needs. Looking to update your current system? I have developed some tools for gap analysis so you can self-diagnose your needs. Need training? I can provide a "live" training session via webinar or in your office if you are in the SF Bay area. Want to discuss? Please directly book a call time by  clicking here . Lazzara 13485:2016 Quality System Document and Services Description Sam Lazzara About Me     sam@lazzara.net      +1 510 397 9739      Directly Book Call Time
Read more