Good Manufacturing Practice, or GMP, is a set of practices and systems that are aimed at making sure that pharmaceutical products are manufactured in conformance with set requirements and standards. The aim of GMP also referred to sometimes as cGMP or Current Good Manufacturing Practice, is to ensure that there is control and consistency in the pharmaceutical products, so that the processes used for controlling quality and consistency of the product can be traced back in the event of a problem.

1. Good Manufacturing Practice
Training
Netzealous LLC
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2. • Good Manufacturing Practice, or GMP, is a set of practices
and systems that are aimed at making sure that
pharmaceutical products are manufactured in conformance
with set requirements and standards. The aim of GMP, also
referred to sometimes as cGMP or Current Good
Manufacturing Practice, is to ensure that there is control and
consistency in the pharmaceutical products, so that the
processes used for controlling quality and consistency of the
product can be traced back in the event of a problem. The
aim of GMP is to implement measures that are aimed at
eliminating risks in the production of the pharmaceutical
product. In this process, cGMP requires manufacturers to
employ the latest available systems and technologies for
complying with regulations.
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3. • GMP covers all aspects of the manufacturing process, right
from the sourcing of the material that go into the product till the
end stage, namely its consumption. The FDA’s GMP
regulations are covered under Chapter IV relating to food, and
under Chapter V, Subchapters A, B, C, D and E for drugs and
devices of the Food, Drug, and Cosmetic Act, and CFR Title
21, Part 210 and 211. The important quality of this regulation is
that it has the power of law, as stated by this Act. So, the FDA
can come down heavily on violators of this law and impose
fines and punishments on them as stated by law. Typically,
failure to comply with the FDA laws on these regulations can
result in recalls, seizure, fines and even jail terms.
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4. Professional trainings relating to GMP
• Good Manufacturing Practice (GMP) regulations are very huge
in number, they are complex, and they have very serious
consequences. This is why it makes sense for pharmaceutical
and food organizations to go through professional trainings that
address the nitty-gritty of GMP. Getting trained on how to
implement GMPs and cGMPs into their business and practice
is an important step to ensuring that the pharmaceutical or food
organization stays compliant with the regulations.
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5. GMP professional trainings from
NetZealous LLC
• NetZealous LLC, a Fremont, CA-based provider of professional
trainings, is a reliable source for understanding the ways in which
GMPs need to be understood and implemented. Trainings from
NetZealous LLC is a very important aid to manufacturers in order
to get their GMPs right, because as we have seen, not getting it
right leads to complications.
• NetZealous LLC’s experts, who are drawn from some among the
best names in the industry, give a thorough understanding of the
way in which GMP practices need to be applied to the industry.
These experts have worked in the industry for many years, and
understand the minutest aspect of the regulation relating to GMP.
NetZealous LLC imparts trainings in the form of webinars,
seminars and in-house trainings to give a complete understanding
of the various aspects of the legislation.
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6. • NetZealous LLC’s experts offer deep and clear understanding of
the elements of GMP, such as:
• Personnel qualifications
• Complaint handling
• Cleanliness
• Equipment verification
• Process validation
• Recordkeeping
• Sanitation
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7. • Plus, NetZealous LLC’s experts also bring a thorough
understanding of all the latest updates that happen in the field of
GMP, as issued by the FDA. In early July of 2016, the FDA issued
a Technical Conformance Guide for Quality Metrics. Aimed at
offering recommendations on data submission for supporting
quality metrics, this guideline is part of the process validation
lifecycle and pharmaceutical quality system assessment. It
addresses issues relating to:
• Electronic submission
• Elements relating to optional and mandatory data
• Rules on data validation
• Specifications relating to the data element
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8. • NetZealous LLC’s experts carry a proper and perceptive
understanding of matters of serious concern for regulatory
professionals, such as these and other updates that keep coming
up from time to time. Getting professional trainings from
NetZealous LLC ensures that the organization stays up-to-date
with whatever is happening in the industry.
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