#Obamacare is on the horizon, but will enough people sign up? http://t.co/WaaiK4BTIb
Big #drugmakers think small with #nanomedicine deals http://t.co/leMPBdZas4 #pharma
Big drugmakers think small with nanomedicine deals
LONDON, May 3 (Reuters) – Is nanomedicine the next big
thing? A growing number of top drug companies seem to think so.
The ability to encapsulate potent drugs in tiny particles
measuring billionths of a metre in diameter is opening up new
options for super-accurate drug delivery, increasing precision
hits at the site of disease with, hopefully, fewer side effects.
Smith & Nephew unveils $300 mln share buyback
LONDON, May 2 (Reuters) – Medical devices maker Smith &
Nephew is to hand back cash to shareholders through a
$300 million share repurchase programme.
The supplier of artificial hips and knees announced the
buyback on Thursday as part of a new capital allocation that
will also see a commitment to continuing investment and
acquisitions.
Europe’s regulator digs in for drug data fight
LONDON, April 30 (Reuters) – The head of Europe’s medicines
regulator is digging in for a fight over data transparency after
being stopped from releasing information on drugs from two U.S.
companies by a court ruling.
Defeat for the European Medicines Agency (EMA) at the hands
of AbbVie and Intermune highlights a growing
battle between campaigners for more openness and companies which
fear it will harm their business.
Interim court ruling stops European Medicines Agency from releasing #AbbVie and #Intermune drug data http://t.co/gIKdlx2WAl #EMA #pharma
Court stops EU regulator from releasing drug company data
LONDON (Reuters) – Europe’s medicines regulator has been stopped from releasing clinical trial data about drugs made by AbbVie and Intermune, following a court ruling favoring the two U.S. companies.
The European Medicines Agency said on Tuesday it intended to appeal the interim decision by the European Union’s general court.
New gene therapy trials aim to mend broken hearts
LONDON (Reuters) – British scientists are stepping up clinical tests of gene therapy in a bid to help people with advanced heart failure pump blood more efficiently.
Researchers said on Tuesday they planned to enroll patients into two new clinical trials using Mydicar, a gene therapy treatment made by privately held U.S. biotech company Celladon.


