May 30 2012
Pharmaceutical
Regulatory Services, Inc. (PRS Inc.), a global provider of
regulatory and pharmacovigilance support to the pharmaceutical,
biotechnology and medical device industries, is pleased to announce the
launch of GRID™
- Global Regulatory Intelligence Database.
In line with our mission to offer our customers the most up-to-date
global regulatory and pharmacovigilance
support services we now offer an online database of pre-approval and
post-approval pharmacovigilance requirements for drugs and biologics in
over 75 countries on all continents. The GRID™ provides an online
reference resource with original national legislative documents for more
in-depth analysis when needed.
Available on cloud technology platform, the database has been developed
and is maintained by the PRS pharmacovigilance experts. The GRID™
database includes information in an easy-to-find grid format with
hyperlinks to the most current reference documents. While the database
is maintained by PRS, clients have the capability to include their own
comments into a client specific comment section.
PRS safety experts search and collect applicable documentation. After
reviewed and analyzed information is entered into the GRID™, E-mail
alert notifications are sent to our clients, including the summary of
the new information in English with links to the original referenced
documents. The GRID database is updated daily and the clients'
pharmacovigilance personnel can access the updated information 24/7, 365
days a year.
Access to this database's innovative technology and daily updates of
changes in global pharmacovigilance requirements saves our customers
significant internal resources while ensuring all their
pharmacovigilance responsibilities can be met. The expansion of GRID
capabilities will continue to be a strategic focus for PRS in the future.
Source: Pharmaceutical Regulatory Services, Inc.