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| What is GMP? |
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| All MSD medicines in the Hong Kong market are
manufactured and supplied from abroad, e.g. Australia,
France, Holland, UK and USA. To bring out our company's
best unique products, the Good Manufacturing Practice
(GMP) requirements are carefully followed in the
MSD production plants. That means regardless of
the type of dosage form , our productions are under
stringent control and quality assured. |
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| The GMP guidelines cover every stage of production,
from processing the raw materials to handling the
finished up. GMP governs manufacturers to have updated
engineering, controlled environment and facilities,
competent personnel and documentation in preparation
of pharmaceuticals. Inspection, chemical testing
and quality control are carried out throughout manufacturing
processes. Thousands of our trained staff work meticulously
to ensure that the composition, potency and efficacy
of each product are consistent from batch to batch.
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Good Manufacturing
Practice |
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A set of principles and procedures, which
followed by manufacturers of therapeutic goods,
helps to ensure that the products are manufactured
with required quality. Various Codes, Guides
and Regulations relating to GMP have been
published by different countries and trade
blocks.
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| GMP provides guideline for the followings
to ensure the quality of a product. |
Manufacturing plant requirements
Equipment requirements
Raw material requirements
Personnel control
Production control
Packing control
Documentation and record keeping
Quality Assurance and Quality Control
(http://www.fda.gov/cder/guidance/4011dft.htm)
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