Top Adding - Writing and Speaking

When you understand what an editor allows in the way of submissions you can begin to see there may be more options available to you than you

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

may have realized. By understanding the ‘big three’ submission types you will find a greater ability to maximize your publishing potential.

; or drug, device, and biological product and fixed dose combination would include two or more combinations of drug.

Examples of combination products may in

What is a Parallel Submission?

When you conduct research for a non-fiction article it is possible to take the research and create several

lude drug-coated devices, drugs packaged with delivery devices in medical kits, and drugs and devices packaged separately but intended to be used together.

rticles on the same topic. This goal can be accomplished through the adaptation of specific word count requirements and a variety of perspec

here is enormous increase in the number of combination products entering the market in the recent years. Combination products have proven advantages but fixe

ives and emphases. These articles are then submitted to publishers – one unique article per submission.

The premise behind this technique i

d dose combinations are still in the process of convincing regulatory authority on their advantages over the single ingredient formulations.

Combination pro

to take the research you performed on the subject and allow it the greatest possibility of publication by allowing a variety of publishers

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

he opportunity to review uniquely written material on a singular, yet well researched topic.

The added benefit is that by writing in a vari

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

ty of styles on the same subject you are continuing the process of fine tuning your ability to wordsmith.

This method is effective because

nation products and maximize the revenues. But the companies involved in this practice are overlooking that they are burdening the patients both economically

ditors often only look at material that is not being sent to another publisher. By providing a unique article to each publication your overa

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

l research is maximized for potential publication.

What are Multiple Submissions?

This term refers to a publisher’s willingness to allow y

ts. Some of the combination products were well accepted by physicians while others suffered. Companies involved in development of combination products are fi

u to send them more than one submission at a time. Multiple Submissions are typically allowed for low word count articles or filler material

ding difficulty in defining their combination products and facing various challenges from selecting a combination to marketing it.

Following aspects would a

These submissions will not take long for the editor to look through so having several to choose from is advantageous for the editor and pro

dd to the challenges in developing combination products:

Which markets to tap where the combination products can do fairly well?
Which combination prod

ides great prospects for you.

What are Simultaneous Submissions?

Many editors will allow an author to provide simultaneous submissions. Th

cts are meaningful and rational?
Which therapeutic categories to select?
Which Combinations can address unmet needs of the patients?
Do combin

s concept allows you to send your work to more than one editor/publisher at the same time. This allows the author another unique opportunity

tions increase the patient compliance?
What would be the developing cost?
How to tackle the risks encountered during combination product developmen

to market their work for potential publication. It should be noted that not all publishers accept a submission that has been sent to another

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

publication while other publishers allow the practice on the condition that the author note the fact in their cover letter.

There’s Just On

ping new procedures for reviewing their safety, efficacy and quality.

Professional from academic institutions, pharmaceutical industries, health care indust

More Thing

Be sure to read through all guidelines whenever submitting material to a potential publisher. Even the kindest editor lacks pat

y and representatives from various regulatory agencies are working out to design the regulatory requirements for manufacture and sale of combination products

ence for a blatant disregard for stated submission guidelines.

You expect the editor to be professional so return the favor. Make sure your

.

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

correspondence is error free, polite and professional in tone. This can go a long way in establishing your ability to interact in a peer to

elopment. They need to be wiser in analyzing the market trends and the regulatory requirements.

Companies that provide selfless information through particip

eer fashion. It also exudes a tone of confidence that can be assistive in allowing the editor to have a similar confidence in your abilities

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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There are many types of Monopolies in Business, Commerce and Industry. Most of the Monopolies that we see are actually created by the Government itself. For one our patent laws enable a company a temporary Monopoly on new emerging technologies, which allows them a head start in trade for putting capital into developing such technologies.

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