Good Manufacturing Practices in Food Industry
Good manufacturing Practices or GMP is what regulates the pharmaceutical industry around the world. GMP training is necessary so that employees in the sector can keep up to date with the new legislation surrounding their work.
Good Manufacturing Practices in Food Industry
Good Manufacturing Practices (GMP) Training and Regulations Around the World
By Sarah Boothman
Good Manufacturing Practices (GMP) are a set or regulations, codes and guidelines governing the manufacture of drugs, medical devices, blood, food and cosmetics. The pharmaceutical industry is interested in those covering the first three groups although corrective cosmetics may also fall under its reach. GMP training is needed to keep manufacturers and their employees up to date with the cGMP or current Good Manufacturing Practices which apply as the most up to date and state of the art regulations. The fact that they are current implies that the practices can change at any moment, which often happens when new technology or advances in research necessitate.
Different countries are subject to the regulation of different authorities.
o In the US the Food and Drug Administration or FDA
o The United Kingdom's pharmaceutical industry is governed by Medicines and Healthcare Products Regulatory Agency (MHRA)
o Therapeutical Goods Administration (TGA) regulates GMP in Australia
These regulatory authorities are charged with inspecting the manufacturing premises of any company involved in the research, trials, production or distribution of any of the products which fall under the GMP jurisdiction. These inspections can be unannounced if the regulatory bodies feel there is just cause to do so. This might occur if a company had a poor report from an organised inspection and they want to make sure that the company has made the necessary changes so that they reach the standards required by GMP.
GMP training is a fundamental part of every employee's work as it helps GMP to become part of the manufacture's everyday life instead of a set of rules that they are constantly trying to achieve. When the cGMP are modified then fresh training is necessary and there may also be structural modifications that need to take place at the production level.
The very reason for Good manufacturing Practices is to ensure that the medicines, medical equipment, blood donations and drugs that humans take are safe. From the very first stage of drug development to the last moment when the drug is prescribed by a pharmacist, GMP regulations ensure that the quality and integrity of the products has not become questionable.
By Sarah Boothman
Good Manufacturing Practices (GMP) are a set or regulations, codes and guidelines governing the manufacture of drugs, medical devices, blood, food and cosmetics. The pharmaceutical industry is interested in those covering the first three groups although corrective cosmetics may also fall under its reach. GMP training is needed to keep manufacturers and their employees up to date with the cGMP or current Good Manufacturing Practices which apply as the most up to date and state of the art regulations. The fact that they are current implies that the practices can change at any moment, which often happens when new technology or advances in research necessitate.
Different countries are subject to the regulation of different authorities.
o In the US the Food and Drug Administration or FDA
o The United Kingdom's pharmaceutical industry is governed by Medicines and Healthcare Products Regulatory Agency (MHRA)
o Therapeutical Goods Administration (TGA) regulates GMP in Australia
These regulatory authorities are charged with inspecting the manufacturing premises of any company involved in the research, trials, production or distribution of any of the products which fall under the GMP jurisdiction. These inspections can be unannounced if the regulatory bodies feel there is just cause to do so. This might occur if a company had a poor report from an organised inspection and they want to make sure that the company has made the necessary changes so that they reach the standards required by GMP.
GMP training is a fundamental part of every employee's work as it helps GMP to become part of the manufacture's everyday life instead of a set of rules that they are constantly trying to achieve. When the cGMP are modified then fresh training is necessary and there may also be structural modifications that need to take place at the production level.
The very reason for Good manufacturing Practices is to ensure that the medicines, medical equipment, blood donations and drugs that humans take are safe. From the very first stage of drug development to the last moment when the drug is prescribed by a pharmacist, GMP regulations ensure that the quality and integrity of the products has not become questionable.
Sarah Boothman is a writer and marketing executive based in Yorkshire, England. She is an avid internet user and likes to share information with the rest of the world. She took part in GMP training whilst working as a pharmacist's assistant. Visit http://www.dba-global.com today.
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