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FMMC 

The FMMC Report

 

          August 1, 2008

 

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In This Issue

 

Chairman's Message 

 

FMMC New Contact Information

 

September Executive Meeting

 July Executive
 Briefing

  

Membership Spotlight

 

 

 

FMMC NEW CONTACT INFORMATION

 

FMMC has a new office!  Please contact and send all correspondence to the location below:
 
325 John Knox Rd, Suite L103 
Tallahassee, FL 32303
 
(866) 437-6534 phone 
 
 (850) 222-3019  
fax 
 

 

 

2008 FMMC Board of Directors


Chairman

Geary Havran  

NDH Medical, Inc. 
 

Treasurer

Alex Stearns 

ETI, Incorporated
 

 

Secretary

Suzanne Christman 
Pinellas County Economic Development 



 

 

 

FMMC 2009 Symposium

Mark your calendars for FMMC's 2009 Symposium on April 7th & 8th at the Tampa Marriott Waterside Hotel & Marina.  Be on the lookout for more information via email or check for updates on FMMC's website at

www.FlaMedMfg.org  

Chairman's Message 

 

Greetings!

 

July saw a very successful Executive Briefing presented by Jayson Bedford summarized below.  Plans are now underway for the next briefing to be held in September.  Please watch your e-mail for the details. 

 

Even as Congress adjourns for their 5 week summer vacation, several actions affecting our industry are in the works.  Please see the article from the law firm of Hyman, Phelps & McNamara, P.C. below for details of one such proposed piece of legislation.


As always, I would like to remind everyone that the value of our association is only as good as the participation of our members.  And speaking of members, please join me in welcoming new member Weiss-Aug Co.  Please forward any comments, suggestions, and offers to volunteer on our various committees to info@FlaMedMfg.org.  Your insights are greatly appreciated. 
 

Sincerely,

 

Geary A. Havran

FMMC Chairman

 September Executive Meeting

 

Details comings soon. 

 

Please log-on to FMMC's website at http://www.flamedmfg.org/upcomingEvents.htm to view more information.


 

 

July Executive Briefing: 

A View from Wall Street
 
 
On July 22nd, the Florida Medical Manufacturers' Consortium (FMMC) resumed their popular series of Executive Briefings with a breakfast presentation from Jayson Bedford, Vice President, Equity Research with Raymond James and Associates.    Based in Clearwater, Mr. Bedford tracks and publishes research on 50+ publicly-traded medical devices companies. 
 
Sponsored by ETI Incorporated, the July breakfast briefing, entitled "How Wall Street Views the Medical Device Industry," provided FMMC members with some very interesting insights into the public medical device industry.  The industry encompasses 135 traded companies with a combined market cap of $700 billion and revenues of $225 billion.  Mr. Bedford noted that Mid-Cap device stocks have substantially outperformed the market, while Large-Cap device stocks have underperformed.  Among some of the key industry trends and challenges, he has observed increased M&A activity and a move toward devices and diagnostics for out-patient care - a product of a tighter reimbursement environment and price pressures.  Mr. Bedford also shared with the group some of the key traits he looks for in medical technology companies and concluded that the U.S. industry offers strong investment opportunities and sustainable growth through innovation.   
 
For a copy of Mr. Bedford's full presentation please click
here

July Executive Meeting

 Sponsored by:

 

ETI logo

 

 

FDA Law Blog

  

 On June 26, 2008, ranking Republican of the U.S. House of Representatives Energy and Commerce Committee, Representative Joe Barton (R-TX), along with several co-sponsors, introduced the "Strengthening of FDA Integrity Act of 2008" (H.R. 6378).  According to an Energy and Commerce Committee Republicans press release, the bill:

  •  Gives FDA the authority to debar any company or individual who is convicted of crimes relating to any drug or device.
  • Gives FDA the authority to debar companies for any misconduct relating to the drug or device, not just over misconduct that takes place during a drug or device's development or approval.
  • Provides great accountability by requiring the FDA to bring debarment actions within one year of the date of conviction. 
  • Requires the FDA to report to Congress on the number of debarment proceedings initiated and imposed each year.

more...

 reprinted with the permission of Hyman, Phelps & McNamara, P.C.

 

Membership Spotlight 

 

New Jersey based Weiss-Aug Co. joins FMMC since establishing Florida presence
 
Weiss-Aug is an ISO 9001:2000 certified company and has extensive experience in developing, prototyping and producing various types of medical devices. Weiss-Aug works closely with major medical device manufacturers in developing components for products such as cannula safety devices, electro-surgical devices, ligature devices, surgical blades, and endoscopic surgical devices. The company year to date has shipped over 7 million molded and 500 million stamped parts, while maintaining strict adherence to customer specifications. Weiss-Aug also provides prototyping, tooling, insert molding, precision stamping, and custom assembly and packaging.
 
Welcome to Florida Weiss-Aug! 

 

For more information on Weiss-Aug Co. please click here.

 

To join FMMC online click here.