FDA seeks comments

August 16, 2011

THE US Food and Drug Administration has issued a draft guidance document to help manufacturers and researchers design “better quality clinical studies in support of premarket approval applications for medical devices”. The document outlines FDA expectations for clinical trial design issues, such as minimising data bias, setting appropriate objectives and choosing study participants.

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Pharmacy Daily | FDA seeks comments

FDA seeks comments

Other recent headlines

Mayne pushes Sun Pharma

Unscripted alcohol debate

LTR secures millions in capital raise

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES