Clinipharma

PG Diploma in Clinical Research

Importance of Post Graduate Diploma in Clinical Research :

Because of growth of industry organizations of clinical trial management and business models have come into existence which includes Contract research Organizations (CROs), early phase CROs, Site Management Organizations (SMOs), companies providing specialized services such as Clinical Data Management, Business Consulting, Knowledge Process Outsourcing (KPOs) etc. This advancement in clinical industry is eventually demanding trained staff in the clinical domain. The post graduate diploma in clinical Research Course is the best choice to enter into the research field. The course is specially designed in a way so as to compliment your basic education and to provide a right platform to make career in Pharmaceutical industry.

What is Clinical Research?

CR is a most knowledge-intensive and interesting field in the pharmaceutical industry. The billion dollar industry is demanding the employment opportunities of qualified and trained professionals in the clinical research sector.

It is categorized into two types mainly

1. Comparative

It is also known as a controlled clinical trial. The research participants are divided into two group's one group receives the investigational treatment, while another group either records the conventional (traditional) treatment or nothing. The control group might be given a fake treatment. This is an idle pill, injection or implantation that seems similar to the investigational treatment. The treatment conducted is kept confidential that means patient and physician both are unaware that who is acquiring the investigational treatment.

2. Open Label

In this type the patient and physician both know that the investigational treatment is going to conduct.

Clinical Industry Scope :

The clinical research industry is encountering awful change worldwide and it is changing in a method for advancement and medication security. This development has composed quality towards advancement of new, one of a kind and more secure treatments and towards customized restorative medications. The pharmaceutical and biotech organizations are quickly venturing up their work in the field of innovative work for building up new particles and also generics.

Significance of Post Graduate Diploma in Clinical Research :

As a result of development of associations of clinical preliminary administration and plans of action have appeared which incorporates Contract examine Organizations (CROs), early stage CROs, Site Management Organizations (SMOs), organizations giving particular administrations, for example, Clinical Data Management, Business Consulting, Knowledge Process Outsourcing (KPOs) and so forth. This progression in clinical industry is in the end requesting prepared staff in the clinical area. The post graduate recognition in clinical Research Course is the best decision to go into the exploration field. The course is uncommonly planned in a path in order to compliment your essential instruction and to give a correct stage to make profession in Pharmaceutical industry.

Classroom Training on Clinical Research

It is the preparation given in a specific organization, instructive firm or in a school. This kind of preparing is exceptionally regular strategy for preparing and it is proffered by numerous understudies to begin their profession in this consistently developing clinical industry.

A career in Clinical Research:

is the way of advancing knowledge about health, illness, and healthcare. There are various types of contemporary career options which you will get in this field. The medical industry is growing exponentially in India and the growth will increase ever after. Some jobs in CR are listed out below

CR associate

CR Investigator

Data manager

Clinical trial auditor

Project manager

Business Development Manager

CR manager

Clinical trial writer

Medical writer

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Phases of Clinical Research Trial

There are main phases of clinical trials: Phase I, Phase II, Phase III and Phase IV. The four phases of the drug approval process are separate clinical trials, and the entire process typically takes eight to 10 years.

Phase I

In this phase the first drug treatment is carried out on a small group of people. Investigator or a scientist figure out the drug's safety, determine a safe dosage range and analyze its side effects.

Phase II

In phase II same procedure is followed as phase one but the treatment is carried out for the large number of people to observe its behavior and safety.

Phase III

The drug treatment is conducted for larger group of people. In this phase scientists or observer confirms effectiveness of a drug on particular disease, monitors its side effects, compare with traditional treatments and gathers all the information about the experiment so that the drug is been used safely in future.

Phase IV

Phase four deals with the post marketing studies that are conducted after a treatment will be approved for commercial use by FDA. Post marketing study includes all the required information about the drug along with its hazards, profits and best usage.