Few Basic Questions Regarding Clinical Research and Clinical Trial

Clariwell is an exclusive platform to dream up a career and flourish the future, this Clinical Research and Pharmacovigilance training is the best selection for the students from life science stream and enthusiastic towards research.
Spread the Word
Listed Under

Clinical Research Course

Affiliate program

Pune - Maharashtra - India

PUNE, India - Dec. 3, 2019 - PRLog -- Few Basic Questions Regarding Clinical Research and Clinical Trial

1. What is clinical research?

Clinical research (http://www.clariwell.in/clinical-research-course-in-pune.php) is the branch of health care where, the research is conducted from the drug discovery till it marketed. In which there are so many phases which will describes the journey of drug discovery.

3. What are clinical trial and the process?

Step 1- found the molecule for targeted disease

Step 2- conduct a pre clinical trial (animal study)

Step 3- submit pre clinical data to regulatory

Step 4- proceed for clinical trial

4. While once the data is generated from pre clinical trial phase are started meanwhile the pre-clinical is consider as phase

Now there are 4 major phases of clinical trial as,

A. phase 1(preparatory phase)

B. phase 2(confirmatory phase)

C. phase 3(therapeutic phase)

D. phase 4(post marketing)

3. What is clinical data management (http://www.clariwell.in/clinical-research-course-in-pune.php)?

Clinical data management is the tool used in clinical research when the data is generated i.e. when subject's visits are done at site level; the generated data is proceeds in CDM on various softwares like MeDra, oracle, etc.

4. What is ICH-GCP?

It's a joint initiative between industry and the regulatory to line up the unique way which follows the standard sets of rules and regulations along with the preferred guidelines which are concern of GCP, ETHICS, and REGULATORY requirements

This guideline are comprises the set of standards as,

1.      Safety  of subject rights and confidentiality is the main concern

2.      The clinical trial should be In accordance with GCP, Ethical requirement and regulatory requirement

3.      Foreseeable risk and benefits of study drugs should be justifiable

4.      IRB reviewed protocol is only consider with compliance one

5.      Everything which is part of clinical trial should be quality assured.

5. What is ICF?

Its inform consent form this is the consent of subject voluntary participation in clinical trial. This is the only document where subject details i.e. the name, address; date of birth is mentioned along with the initials for identification.

In this concept the clinical trial background and general information is given to subject about the drug and study design, compensation, policies etc.

Ethics committee and the PI details are given through this consent

This is the only document which is not transferable to anyone to maintain the confidentiality of subject (patient) details that's why this document is most important while participating a subject into the clinical trial (http://www.clariwell.in/clinical-research-course-in-pune.php).

Media Contact
Zain Malik
Tags:Clinical Research Course
Industry:Affiliate program
Location:Pune - Maharashtra - India
Account Email Address Verified     Account Phone Number Verified     Disclaimer     Report Abuse

Like PRLog?
Click to Share