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Just Answers - Article Directories And Directory Submission Guidelines III
You might find that if you use HTML where it is not allowed, and the submiss
According to USFDA, a combination product is one composed of any combination of a drug and device; biological product and device; drug and biological product
ions are not manually checked or edited, your article could be sent out in p
; or drug, device, and biological product and fixed dose combination would include two or more combinations of drug.
Examples of combination products may in
Examples of combination products may in
lain text format with all your HTML tags showing. This makes you look very
lude drug-coated devices, drugs packaged with delivery devices in medical kits, and drugs and devices packaged separately but intended to be used together.
amateurish, and should be avoided. Many authors never bother to use HTML ex
here is enormous increase in the number of combination products entering the market in the recent years. Combination products have proven advantages but fixe
cept in some specific directories that they manually submitted to when using
d dose combinations are still in the process of convincing regulatory authority on their advantages over the single ingredient formulations.
Combination pro
Combination pro
HTML formatting.
Always make sure you know of any minimum and maximum word
Always make sure you know of any minimum and maximum word
ucts have become life saving products for the pharmaceutical companies who doesn’t have many innovative molecules in their product pipeline and have been inc
count limitations in the body text and the resource box. If there are, and
easingly used in the product life cycle management. Even the companies having product patents are trying to extend their product life cycle through the combi
you don’t stick to them, your text will be truncated at the maximum count.
nation products and maximize the revenues. But the companies involved in this practice are overlooking that they are burdening the patients both economically
With respect to resource boxes, not all directories offer them. You might b
and physically. They need to rightly judge the benefits of the combination products and they have to even look at the risks involved when combining the produ
e allowed links to your website but they have to be included at the end of t
ts. Some of the combination products were well accepted by physicians while others suffered. Companies involved in development of combination products are fi
he article. Be careful with this or your automatic submission could end up
ding difficulty in defining their combination products and facing various challenges from selecting a combination to marketing it.
Following aspects would a
Following aspects would a
with nothing linking back to your site because your bio box has not been inc
dd to the challenges in developing combination products:
Which markets to tap where the combination products can do fairly well?
Which combination prod
Which markets to tap where the combination products can do fairly well?
Which combination prod
luded.
Every directory will have its own guidelines since there is no unive
Every directory will have its own guidelines since there is no unive
cts are meaningful and rational?
Which therapeutic categories to select?
Which Combinations can address unmet needs of the patients?
Do combin
Which therapeutic categories to select?
Which Combinations can address unmet needs of the patients?
Do combin
rsally accepted format for article submission. Take your time to understand
tions increase the patient compliance?
What would be the developing cost?
How to tackle the risks encountered during combination product developmen
What would be the developing cost?
How to tackle the risks encountered during combination product developmen
those for all the directories you submit to; auto-submissions are not always
t?
As combination products don't fit into the traditional categories of drugs, medical devices, or biological products, the USFDA is in the process of devel
As combination products don't fit into the traditional categories of drugs, medical devices, or biological products, the USFDA is in the process of devel
able to take this into account. Sometimes submitting one article to hundre
ping new procedures for reviewing their safety, efficacy and quality.
Professional from academic institutions, pharmaceutical industries, health care indust
Professional from academic institutions, pharmaceutical industries, health care indust
ds of different sites just does not work, due the number of different submis
y and representatives from various regulatory agencies are working out to design the regulatory requirements for manufacture and sale of combination products
sion rules applied by the various directories.
Read what the directory subm
Read what the directory subm
.
As there is an increasing trend of the combination products companies manufacturing such products should be able to tackle the problems involved in the de
As there is an increasing trend of the combination products companies manufacturing such products should be able to tackle the problems involved in the de
ission guidelines permit then take advantage of them. You should be able to
elopment. They need to be wiser in analyzing the market trends and the regulatory requirements.
Companies that provide selfless information through particip
Companies that provide selfless information through particip
make maximum use of the features that each of the article directories allow
tion in industry events and feedback to regulatory authorities would be able to face the challenges and will be successful in developing combination products
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