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'Trademark Clearinghouse' for new gTLDs to open March 26
- Fish & Richardson PC
- -
- USA
- -
- February 26 2013
The avalanche of new generic top-level domain names will soon be upon us. Trademark owners will need to contend with the prospect of cybersquatting
gTLD comment period extended
- Fish & Richardson PC
- -
- USA
- -
- August 15 2012
Thought you missed your chance to submit comments regarding a new gTLD application?
New gTLD "reveal day" has arrived
- Fish & Richardson PC
- -
- Global
- -
- June 13 2012
Today, the new gTLD applications list, including applicant information and character strings, has been posted at www.icann.orgreveal
New gTLD "reveal day" is June 13 - are you ready?
- Fish & Richardson PC
- -
- Global
- -
- June 4 2012
More than 1,200 companies have applied for more than 2,000 new generic top-level domain names (gTLDs) to compete with .com, .org, etc
Another chance at .xxx
- Fish & Richardson PC
- -
- USA
- -
- February 10 2012
Were any of your company's Sunrise A or Sunrise B .xxx priority domain name applications rejected?
Is your company ready for ".anything"?
- Fish & Richardson PC
- -
- Global, USA
- -
- December 15 2011
The Internet as we know it may soon be changing forever
New gTLD applications accepted in early 2012
- Fish & Richardson PC
- -
- USA
- -
- November 28 2011
The Internet as we know it may soon be changing forever
.xxx opt-out deadline fast approaching!
- Fish & Richardson PC
- -
- Global, USA
- -
- October 24 2011
Trademark owners who do not want new “.xxx” Internet domain names to be based on their registered marks should file their blocking applications as soon as possible
Reminder: limited opt-out period for .xxx domain names
- Fish & Richardson PC
- -
- USA
- -
- September 7 2011
Trademark owners who do not want new “.xxx” Internet domain names to be based on their registered marks may now file blocking applications through October 28
Your software may be a ‘medical device’ subject to FDA regulation
- Fish & Richardson PC
- -
- USA
- -
- August 10 2011
In late July 2011, the FDA released a draft guidance document outlining when certain types of software would be considered a “medical device” subject to FDA scrutiny
