News & Analysis on Clinical Trial Services & Contract Research And Development
Despite questions over India’s regulations governing clinical trials, the largest CROs in the world do not seem deterred from running trials there, according to a recently released list of global trial approvals from 2012.
Constantly evolving IT systems and tech innovations make clinical trial data harder to manage than manufacturing info, says Comprehend Systems.
The UAE says it will allow generic drug manufacturers to import active ingredients of patented drugs to encourage local industry growth.
The US FDA has sent Wockhardt a warning letter for its manufacturing plant in Waluj, India just days after UK authorities issued the site with a certificate of non-compliance.
Import duties on some pharma intermediates could be suspended temporarily under legislation being debated in the US House of Representatives.
Accenture is using its consulting and tech expertise to corner the R&D service market with a slightly different style than CROs typically use.
US CBO claims that proposed track and trace legislation will not be too expensive for drugmakers already used to similar laws in California are ‘misguided’ according to an industry consultant.