Veeda Clinical Research - Phase 1 Clinical Research, CRO
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Home » What is a clinical trial » FAQs
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Clinical Research,Phase I/II studies
About Veeda Clinical Research

FAQs

 
What are the different phases of clinical research?
 
Is it safe?
The safety and well-being of all volunteers at Veeda CR is the primary concern of the clinical staff, all of whom are highly trained professionals in their field of expertise. All drugs must be rigorously tested, firstly in the laboratory and then in animal studies before being given to healthy volunteers, and then in healthy volunteers before they can be given to patients.
 

Taking any medication, either prescribed by your own GP or those available over the counter, may present a risk. At Veeda CR we work hard to minimise any risks by vigorously scrutinising animal data, thoroughly screening our volunteers to ensure they are fit and healthy enough to take part in a clinical study and also by close monitoring volunteers throughout the study.

 

It is also important volunteers are totally honest at the screening stage when giving their medical history and follow the guidelines given by the clinical staff throughout the study.

 
Everything we do is governed by the MHRA (Medicines and Healthcare Products Regulatory Agency) which is a government regulatory authority, and an independent Ethics committee.
 

What is involved in being a volunteer?

 

Who can become a volunteer?

 

Are there any restrictions?

 

Are visitors allowed?

 

Can I withdraw from a study?

 

What happens to my personal data?

 

What is in it for me?

 

How often can I take part in a trial?

 
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