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  • Actual - No Duplicate Title Rules on Online Article Submission Websites

    Some of the top online article submission web sites do not allow duplicat
    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
    e titles on the articles that they accept from article authors and articl
    ; or drug, device, and biological product and fixed dose combination would include two or more combinations of drug.

    Examples of combination products may in
    marketers. Does this rule makes sense? A few article marketers have comp
    lude drug-coated devices, drugs packaged with delivery devices in medical kits, and drugs and devices packaged separately but intended to be used together.

    ained because they save the best titles have already been taken.

    Of cour
    here is enormous increase in the number of combination products entering the market in the recent years. Combination products have proven advantages but fixe
    e this really only happens on those online article submission sites that
    d dose combinations are still in the process of convincing regulatory authority on their advantages over the single ingredient formulations.

    Combination pro
    ave over 300,000 articles and perhaps over 30,000 article authors. With t
    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
    at huge number of articles and authors it makes sense that there will be
    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
    the occasional conflict. But how often does this actually happen?

    Well,
    nation products and maximize the revenues. But the companies involved in this practice are overlooking that they are burdening the patients both economically
    n one of the top online article submission websites that has this rule; I
    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
    never seem to have to change titles, but there were 6 priors when they in
    ts. Some of the combination products were well accepted by physicians while others suffered. Companies involved in development of combination products are fi
    tituted that rule, I guess I would have had priority, since in 5 of the c
    ding difficulty in defining their combination products and facing various challenges from selecting a combination to marketing it.

    Following aspects would a
    ses I was a member of the online article submission web site team and lis
    dd to the challenges in developing combination products:

    Which markets to tap where the combination products can do fairly well?
    Which combination prod
    of authors first, but I did not mind changing them. Today, I am very car
    cts are meaningful and rational?
    Which therapeutic categories to select?
    Which Combinations can address unmet needs of the patients?
    Do combin
    ful to make longer titles or tricky ones to prevent this. It has not been
    tions increase the patient compliance?
    What would be the developing cost?
    How to tackle the risks encountered during combination product developmen
    a problem at all for me.

    Still there are a few article authors and arti
    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
    le marketers who consistently write very short titles of two to three wor
    ping new procedures for reviewing their safety, efficacy and quality.

    Professional from academic institutions, pharmaceutical industries, health care indust
    s and they have conflicts quite often because there are only so many comb
    y and representatives from various regulatory agencies are working out to design the regulatory requirements for manufacture and sale of combination products
    nations that can be used. Nevertheless I think the rule of no duplicate
    .

    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
    itles makes sense. It prevents confusion from the reader and actually he
    elopment. They need to be wiser in analyzing the market trends and the regulatory requirements.

    Companies that provide selfless information through particip
    ps the article authors in the long run. Please consider all this in 2006


    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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