Covance picked up a Good Laboratory Practice Certificate for its Shanghai early development facility, a regulatory milestone the CRO says gives it a leg up on global competitors.
Alimera Sciences is facing an uphill battle getting its chronic diabetic macular edema drug on shelves in Europe, and now the company has recruited Quintiles to manage the European launch of Iluvien.
Amid budget-slashing and restructuring, AMRI has some good news to report: The CRO has re-signed with GE Healthcare to supply materials for diagnostic imaging, locking down its biggest commercial supply client through 2016.
CMO NextPharma has sold its U.S. manufacturing operation, Bioserv, to private equity player KESA Partners for an undisclosed sum, planning to focus on its core European operation.
Vaccine outfit Selecta Biosciences has signed an agreement with Sanofi to discover antigen-specific immunotherapies for food allergies, and the deal includes rights to an initial therapy with the option to develop two more.
Thanks to lax regulations and legal loopholes, Indian regulators have little control over the conduct of CROs in the country, but the government is on the path to reforms that would help rein in "fly-by-night" trial operators, officials said.
Parexel International is adding another academic partner to its list of overseas collaborators, inking a deal with the National Taiwan University Hospital to provide drug development services in the country.
The majority of Big Pharma companies use CROs to conduct clinical trials in the developing world, but very few could provide evidence that they'd ever disciplined contractors that ran afoul of ethics codes, possibly putting participants at risk, according to a study by the Access to Medicine Foundation.
CRO AMRI is closing up its R&D shop in Bothell, WA, and shipping the site's biology capabilities to its drug discovery operation in Singapore.
Big Pharma seems to be feeling the spirit of collaboration of late, and Pfizer and AstraZeneca have joined forces to launch the Néomed Institute, a nonprofit drug R&D outfit that will unite CROs, schools, biotechs and VCs to develop and commercialize new therapies.
CRO Medpace has bought MediTech Strategic Consultants, a European contract researcher that specializes in medical device R&D.
The EU is looking to liberalize its clinical trial regulations to spur drug development in the Continent, and the U.K.'s Medicines and Healthcare products Regulatory Agency (MHRA) wants to hear from CROs and drugmakers on the proposed reforms.
QPS is adding 24 beds to its Phase I facility in Groningen, Netherlands, citing an increase in demand for its quick-turnaround, complex research.
China's Innovent Biologics is looking to build the largest GMP biologics plant in China, a belt currently held by WuXi PharmaTech, and the company has $25 million in new investments to get it done.
Chinese CRO ShangPharma posted a 39.5% drop in net income in the third quarter, as increasing costs tamped down a 10.6% rise in net revenue.
As clinical trials get more and more complex, Pharmaceutical Product Development has reached out to technology consultancies Tessella and Berry Consultants to use FACTS, adaptive trial software that lets study designers simulate trials in their early planning stages.
Catalent is cutting 45 jobs from its Swindon, U.K., facility, a move the company told a local newspaper is part of a restructuring effort at the site.
Earlier this year, 10 of the biggest names in drug development joined forces to streamline outsourcing R&D, and the resulting nonprofit is creating a huge database of global clinical trial sites.
It's been a banner week for New Jersey CRO Chiromics, as the company's chemical compound library has enticed Big Pharmas Bristol-Myers Squibb and GlaxoSmithKline.
Aptuit and GlaxoSmithKline have agreed to extend their partnership for another two years, a move Aptuit says is a validation of its drug discovery efforts.