Blog
Pathways’ Bowker leads FDA supplier audit webinar
Are you a supplier of raw materials, component parts or finished product to biopharma or medical device companies? The supply chain for pharmaceuticals, biologics and medical device companies are increasingly being audited by their clients and FDA. On July 25, 2013,...
EMA Draft transparency policy open to public for comments
An article posted on clindev.eu shares that the European Medicines Agency (EMA) has announced a three month public consultation of a draft transparency policy regarding clinical trial information. EMA is hoping to launch the policy in early 2014. Potential threats to...
Successful open house for Pearl Pathways
Pearl Pathways’ open house last Thursday the 20th welcomed in the new office with a bang. The afternoon get together was a fun way for visitors to stop by and see the new place. A refurnished interior to an old Indianapolis building on the south side of the city...
Global data sharing in genomics in the works
FierceBiotechIT.com journalist Ryan Mcbride shares that an alliance with close to 70 organizations has been formed to improve how genomic and clinical data are managed and shared. This alliance is a response to how ineffective big data sharing has been for people...
Health IT solutions to be the topic of IHIF June lunch series
Health It solutions are critical to an organizations success and will also be the topic of the IHIF June lunch series. The discussion will pertain to helping coordinate patient information, addressing challenges in healthcare delivery, and reducing costs of clinical...