Running Head: PHARMACOLOGY 1

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Pharmacology

I. Discuss the process and regulations of Fast Track.

Fast track refers to an expedited procedure concerning congressional consideration

regarding trade agreements (Great Britain, 2014).  It necessitates congress to vote on an

identified agreement without undertaking reopening any of fast track provisions. It entails three

fundamental features which are an up or either a down vote that lacks amendments as well as

extensive consultations along with coordination with congress throughout the entire process and

a vote on the implementation of the legislation within a specific period of time. The process of

fast track is for noncontroversial regulations.

The regulation process begins with adoption of a fast track regulation. Thereafter, there is

executive branch review which is followed by contacting of the clerks associated with the House

along with the Senate directly for verifying which committees need to be notified regarding the

action. Fast track is usually published in the identified registrar (Great Britain, 2014). The

regulation regarding fast track becomes effective 15 days after the close of the public associated

forum.

II. Identify which medical conditions warrant the use of “Fast Track” drugs.

There are a variety of medical conditions which warrant utility of fast track drugs. Fast

track drugs are utilized under rare fatal as well as life threatening illnesses and disorders which

are associated with tremendous challenge in the transformation of scientific related discoveries.

To warrant the utility of fast track drugs in treating medical conditions entails putting into

consideration a variety of aspects regarding such a condition such as its severity as well as rarity

and prevalence regarding the condition as well as the availability or unavailability of alternative
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methods of treatment. Therefore, fast track drugs are utilized under fata medical conditions with

sever effect on identified surrogate end point as they are considered efficient and most effective

(Ballweg & Vetrosky, 2017). 

Hi Thalia great post

To warrant the utility of fast track drugs in treating medical conditions entails putting into

consideration a variety of aspects regarding such a condition such as its severity as well as rarity

and prevalence regarding the condition as well as the availability or unavailability of alternative

methods of treatment. Fast track drugs are utilized under rare fatal as well as life threatening

illnesses and disorders which are associated with tremendous challenge in the transformation of

scientific related discoveries. (Ballweg & Vetrosky, 2017).

Fast track is usually published in the identified registrar The process of fast track is for

noncontroversial regulations. Thereafter, there is executive branch review which is followed by

contacting of the clerks associated with the House along with the Senate directly for verifying

which committees need to be notified regarding the action. The regulation process begins with

adoption of a fast track regulation. (Great Britain, 2014).

References

Ballweg, R., Brown, D., & Vetrosky, D. (2017). Physician Assistant: A Guide to Clinical

Practice E-Book.

Great Britain., & Great Britain. (2014). Fast-track legislation: Constitutional implications and

safeguards : 15th report of session 2008-09. London: Stationery Office.

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