Regulations Globally Harmonized System

Written in everyday language, it clearly describes employees roles and responsibilities regarding every element of hazard communication and the Global Harmonized System (GHS). It even goes beyond the regulations to provide practical information on labeling. Safety Data Sheets, common acronyms and abbreviations, and day-to-day best practices. 

The information given to the user by a chemical s label is concise and precise. The constituent elements are regulated, based on the recommendations of the Globally Harmonized System. 

According to European parliament regulation 1005/2009, the use of any solvent with the H420 (harms public health and the environment by destroying ozone in the upper atmosphere) hazard phrase in the Globally Harmonized System (GHS) of Classification and Labelling of Chemicals is severely restricted. 

Change from old CHIP (Chemicals Hazard Information and Packaging) to new GHS (Globally Harmonized System of Classification and Labeling of Chemicals) regulation... 

The new medical device regulations were codified in 1996, significantly altering the way in which medical device manufacturers were inspected by the FDA. The quality systems inspection technique (QSIT) was launched as part of the new strategy for inspecting the device industry. This inspection technique allowed FDA to move closer to global harmonization guidelines... 

With the enforcement of the revised PAL and relevant regulations, ICH harmonization and globalization of drug development will bring a new era for drug development and reviewing system of NDAs so that Japan will become a full member of the countries in the long run. 

There is variability between regnlators on the characteristics of software systems which constitute being a medical device and the Global Harmonization Task Force has gone some way to standardising definitions [64]. In practice HIT systems which fall into medical device regulation typically include ... 

---