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Food additives

Food additives are chemicals added to foods to keep them fresh or

to enhance their colour, flavour or texture. They may include food colourings (such as tartrazine or cochineal), flavour

enhancers (such as MSG) or a range of preservatives.

Safety tests for food additives

Food Standards Australia New Zealand (FSANZ) is responsible for the approval of which food additives are

allowed in Australian foods. All food additives used in Australia undergo a safety assessment, which includes rigorous

testing before they are approved.
Toxicological tests on animals are used to determine the amount of the additive that is expected to be safe when consumed

by humans. This is usually an amount 100 times less than the maximum daily dose at which ‘no observable effects’ are

produced by an additive consumed over the test animal’s lifetime.
If there is any doubt over the safety of an additive, approval is not given. If new scientific information becomes

available suggesting that a food additive is no longer safe, the approval to use the food additive would be withdrawn.

Most food additives are tested in isolation, rather than in combination with other additives. The long-term effects of

consuming a combination of different additives are currently unknown.

Plant Extracts: The Original Food Additives

Plant and herb extracts have long been used to enhance the healthfulness, color, and even taste and flavor of foods,

beverages and supplements. With an often “natural” positioning, their popularity is assured.

Ginny Bank, Contributing Editor

October 2011/NutraSolutions -- In 399 BC, the Greek philosopher Socrates was executed by drinking an infusion of

the poisonous hemlock plant. In ancient Egypt, Cleopatra used henbane extract to dilate her eyes and make her appear more

alluring. Also in Egypt, red fabric found in the tomb of King Tut contained alizarin, a pigment extracted from the roots of

the madder plant. While such historical accounts documenting human use of plant-based extracts can be traced back over

3,000 years, their use is possibly as old as civilization itself. From the very first Chinese dynasties, Mesopotamia and

ancient Greece, and westward to the empires of Mesoamerica, early civilizations had a surprisingly sophisticated

understanding of botanicals and their extracts, especially for use as medicine. Flowers, fruits, roots, bark and leaves of

plant material were extracted by various techniques to concentrate not only their therapeutic properties, but also their

pigments, aromas and flavors. The simplest method of extraction, used for plants that have high oil content, was the

expression of the essential oils. Other techniques included steeping the plant part in water to make an infusion (also

known as a tisane) or mashing them and boiling in water to make a decoction. This method was also used to make natural

dyes, sometimes boiling the decoction for days to concentrate the pigments further. Elixirs were produced by extracting the

plant parts in alcoholic beverages to dissolve the active components.

Today, the use of plant extracts to flavor, color and improve

health are not that different from ancient times. Even the extraction methods are fundamentally the same. And, with

hundreds, if not thousands, of years of traditional use behind many plant extracts, their safety (and often their efficacy)

has been well-documented. Even so, when one takes into account the massive number of plant-based extracts used in

traditional medicinal systems, such as Ayurveda and traditional Chinese medicine, very few are approved for use in foods or

have Generally Recognized as Safe (GRAS) status. This may be changing, as self-affirmation of GRAS status for such

ingredients is steadily increasing. Within the last 18 months alone, a number of extracts received GRAS status through

self-affirmation, with or without FDA notification

Pharmaceutical manufacturing is a strictly regulated, process-driven industry. A mistake in manufacturing can be costly in

the best-case scenario and at worst, it can be life-threatening, particularly if a product has reached consumers.

The industry must adhere to numerous guidelines that are laid out by the Food & Drug Administration (FDA), for example,

the Current Good Manufacturing Practices (cGMP). Product quality is at the center of cGMP, which assures the

correct monitoring, design, and control of manufacturing facilities and processes.

cGMP also supplies guidance for how to attain quality raw materials, in addition to the preferred management processes

and systems for maintaining optimum laboratory testing procedures. All factors play a key part in the effectiveness and

safety of pharmaceutical raw materials.

For manufacturers, adherence to cGMP is a necessity, and while quality and safety are top priorities in the

pharmaceutical industry, these guidelines do introduce more challenges in the manufacturing process. 

Medical apparatus and instruments refer to

instruments, instruments, implants, extracorporeal reagents or similar or related items used to diagnose, prevent or treat

diseases or other medical conditions, and are not achieved by chemical effects (such as drugs) in the body or in the body

Its purpose. The main goal of any medical device is to improve the patient’s daily quality of life or well-being during

diagnosis, treatment, and/or medication. Over the last decade, the medical device industry is a fast-growing and

demanding industry. Advances in design, materials, and technologies have increased the potential to develop improved

solutions for all medical applications. These advances have managed to supply the clinicians with new products, tools,

and procedures, supporting them in their work by making surgery, diagnosis, or treatment processes easier than ever

before. These advances have also aimed to reduce both lead times and costs in the production of existing medical

devices, reducing global healthcare costs. Due to this fact, medical devices are a hot topic among the industrial and

academic domains regarding issues such as design, materials, prototypes, or manufacturing processes.

Fine and specialty chemicals are a not sharply defined chemical substances that are usually produced in small

quantities and on special customer request. Fine chemicals are

chemical substances that are obtained by means of complex syntheses and have a guaranteed degree of purity. Specialty

chemicals is the broader term and generally includes chemical substances for special applications where the effect is what

counts most. 

You can use disposable protective gloves to

protect your hands from any kind of hazard. There are three main types of disposable safety gloves. There are latex gloves,

which are manufactured from natural rubber. Nitrile gloves are produced from synthetic nitrile rubber. And vinyl gloves are

made from synthetic plastic polymer. Whichever type of glove you decide to use, you should always ensure that it is

suitable for your kind of industrial application. Disposable gloves are usually manufactured with a service grading. The

service grade of a disposable glove indicates the type of industry that it should be used. This article looks at the

various uses of disposable gloves according to industry.

 

Medical Usage


Disposable safety gloves are some of the most commonly used safety products in the healthcare industry. These gloves

are worn to prevent cross-contamination between patients and medical staff. They are also used for general hand protection

when handling various sensitive things in a medical setting. Disposable gloves that are used in the healthcare industry are

referred to as medical gloves. Medical disposable gloves are tested and approved by the U.S. Food and Drug

Administration (FDA). These gloves are worn by surgeons, doctors, laboratory technicians, nurses, caregivers, dentists and

all other medical personnel. Blue disposable gloves are most popular for healthcare use, but you can also get

medical safety gloves in various shades of pink, purple, and even grey. These gloves undergo several rounds of testing

including leak and puncture testing, and visual defect examination. The FDA allows only premium grade medical safety gloves

to be marketed.

 

Food Service Usage

There are special disposable gloves for use in the food service industry and restaurants. These gloves are also tested

and approved by the FDA. Food service gloves are worn by chefs, waiters, and various hospitality personnel. Food service

gloves are used to prevent cross-contaminating during food preparation and service. Like the medical disposable gloves

discussed above, food service gloves undergo serious testing before they can hit the market. Food service gloves are

usually white in color to Accenture the cleanliness or sterility of the hospitality industry.

  • Created: 11-08-21
  • Last Login: 11-08-21

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