RMH
pixel skylines
ellievsbear
Not today Justin
EXPECTATIONS
Kiana Khansmith
art blog(derogatory)
#extradirty
Sade Olutola
No title available
Misplaced Lens Cap
Today's Document
shark vs the universe
JVL
we're not kids anymore.
tumblr dot com
Lint Roller? I Barely Know Her
YOU ARE THE REASON
if i look back, i am lost
Monterey Bay Aquarium
seen from Ukraine
seen from Singapore
seen from Netherlands
seen from Argentina
seen from Germany
seen from Netherlands
seen from United Kingdom
seen from Fiji
seen from United States
seen from Spain
seen from Russia
seen from Türkiye
seen from United States
seen from Germany
seen from Dominican Republic
seen from Egypt
seen from Malaysia
seen from Russia
seen from Argentina
seen from United States
@clinicalocean
How to Search Patient or CRF in Long Lists of RDC On-site
Last time in RDC On-site we learned navigation from one page to another. Now today I will show you some tip and trick for searching patients or CRF in RDC and how you can see long lists in a same page without navigating to other pages. Well, basically RDC shows you only 50 patients within a page...
http://bit.ly/1tz7LIP
25+ Clinical Trial Management Systems (CTMS) - What is you choice
Clinical Trial Management System is a computer application or web based application. Now these days, when clinical trials are continuously increasing all over the world, CTMS play very important role to boost-up the process and reduce time taken by any clinical trial. Most of the biotechnology, …
http://clinicalocean.com/2014/09/24/clinical-trial-management-systems-ctms/
New Post has been published on http://clinicalocean.com/2014/09/20/good-clinical-data-management-practices-complete-guide/
Good Clinical Data Management Practices - Complete Guide
Clinical Data Management is one of the main pillar in any Clinical Trials or in Clinical Research. On the other hand Good Clinical Data Management Practices boost its quality and work flow speed.
GCDMP is a regulatory guidelines or company standards for clinical data management. According to this all the data from clinical trials phase, clinical labs and from complete clinical research should be collected and converted into digital form for fast analysis and reporting purposes.
U.S. Food and Drug Administration and International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals of Human Use have developed these regulations and guidelines for drug and device development process.
Society of Clinical Data Management (SCDM) has created a complete guide for good clinical data management practices. GCDMP guidelines are updated by Subject Matter Experts on regular basis.
I have collected the same document and thankful for SCDM. If you want this complete guide then please file below form then I will send you this document in your mailbox.