Product News
January
2008
cGARD 4.1 Auto - Release - ICH standards, UK &
Chinese regulations added! - 11/01/08
As our tool evolves and becomes more and more
popular within the industry (8 out of 10 top global pharmaceutical
companies use cGARD), we are constantly working on improvements and
enriched up-to-date regulatory content of cGARD.
Based on customer feedback and continuous
development strategy, the database has been enriched with several
key industry standards and regulations from ICH, UK and China!
For the benefit of our current customers, our tool
is now being released via automatic update function embedded within
cGARD. We have also implemented a secure method of purchasing cGARD
online.
More and more companies are interested in China as
a potential source of business and production, therefore cGARD will
now include key regulations from that market to help interested
professionals to access up-to-date regulatory information within
seconds.
Also we have spotted that industry is shifting
towards a standardized approach and ICH standards are becoming key
documents that determine rules within the life science world.
Finally, based on feedback from several clients, we have input key
regulations from the UK market.
New automatic database update includes:
Complete set of ICH
standards
Regulations from UK:
MHRA - 2005/2789 - The Medicines for Human Use (Manufacturing,
Wholesale Dealing and Miscellaneous Amendments) Regulations 2005
Regulations from China:
Drug Administration Law of the Peoples
Republic of China
Regulations for Implementation of the Drug
Administration Law of the Peoples Republic of China
Regulations for
Supervision and Administration of Medical Devices
Regulations on
Administrative Protection for Pharmaceuticals
The database now contains 10,090 records of
global, up-to-date and categorised regulatory information.
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