Pharmaceutical
Regulatory Services, Inc. a worldwide supplier of regulatory and
pharmacovigilance support into the pharmaceutical, biotechnology and medical
device industries is delighted to declare the launch of GRID™ - Global
Regulatory Intelligence Database. According to our mission to provide our
customers the foremost up-to-date global regulatory and pharmacovigilance
support service all of us now offer an internet database of pre-approval and
post-approval pharmacovigilance specifications for drugs and biologics in over
75 nations on all continents. The GRID™ presents an online reference resource
by using original national legislative documentation for more in-depth research
if needed.
Present
on cloud technology platform, the database is developed and is kept by the PRS
pharmacovigilance experts. The GRID™ database has information in an
easy-to-find grid format along with hyperlinks to the most current quotation
documents. As the database is checked by PRS, clients possess the capability to
actually include their very own comments into a client specific remark section.
PRS
safety specialists explore and collect applicable documentation. After reviewed
and diagnosed details are entered into the GRID™, E-mail alert notifications
are delivered to our clients, which includes summary of typical new information
in English with hyperlinks to the unique referenced documentation. The GRID
database is up-to-date daily as well as the clients' pharmacovigilance
personnel can access the up-to-date information 24/7, 365 days a year.
Having
access to this database's innovative technology and day-by-day updates of
changes in worldwide pharmacovigilance requirements spares our client’s
significant inside resources whereas ensuring all of their pharmacovigilance
responsibilities might be met. The expansion of GRID attributes will still be a
strategic focus for PRS in the future.
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