Good Distribution Practice Discussion 2022

Reading Head: GOOD DISTRIBUTION PRACTICE
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Psycholo
gy
April 11
202
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GOOD DISTRIBUTION PRACTICE 1
Contents
Introduction................................................................................................................................2
Goods Distribution Practice.......................................................................................................2
Good Manufacturing Practice of Pharmaceutical Products....................................................2
Storage of Pharmaceutical Products.......................................................................................4
Recommendations......................................................................................................................5
Conclusion..................................................................................................................................6
References..................................................................................................................................7

GOOD DISTRIBUTION PRACTICE 2
Introduction
Good distribution is considered to be that practice in which the government has set some
regulatory guidelines that help in governing the wholesale distributors of the product. This
practice is considered to be an essential part. It is because it is concerned with the quality
assurance. This practice will help in ensuring the quality of pharmaceutical products. It is
very important to maintain the quality of these products as they are concerned with the health
of the people. Many activities are involved in the goods distribution process. This process
includes manufacturing, storage, transportation, import and handling activities (bsi., 2020).
In this discussion, the main focus will be on two factors of good distribution practice. These
factors are Goods manufacturing practices and storage of pharmaceuticals products.
Goods Distribution Practice
Goods distribution Practice is considered to be an essential element that helps in evaluating
quality assurance. Therefore it is required by every company to initiate a quality system that
ensures that products are properly stored and handled. Certain appropriate conditions are
been required in the organizations (HSA, 2019).
Good Manufacturing Practice of Pharmaceutical Products
This is considered to be the system that helps in ensuring the manufacturing of
pharmaceutical products. The products that are included in this category are food, cosmetics,
and pharmaceutical products. All these products need continuous process and quality should
also be maintained. Some regulations are implemented by the government to maintain the
quality of the products. These regulations are implemented by manufacturers all over the
world. These are also considered to be essential regulations that can regulate the
manufacturing, verification, and validation of products (Focused Pharama Engineering,
2020). Twelve basic guidelines are have followed by the companies in Singapore. These
guidelines are as follows:
 Quality Management
The principle of quality management is used for ensuring that the products are safe to use and
it will fulfil the requirement of patients. It will also ensure that there is no risk in consuming
these products. The factors that are used in this principle are quality assurance, quality
control, GMP for product and risk management (integrating GMP, 2005).