Nick Paul Taylor from fiercebiotechit.com provides a unique look at how biopharma companies are moving from paper clinical trial data to electronic files. The article talks about how many vendors are now pushing the electronic filing method for a variety of reasons including the ability to easily share clinical study documents in a safe and secure way. Normal clinical trials can require up to 25, 0000 documents which can create a huge logistical issue that sponsors and service providers are failing to meet. To read the full article click here.