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Clinic Trial Management Services

Offering you a complete choice of services which include SMO Services, Patient Recruitment, FAQ Management Service and Principal Investigator Recruitment.

SMO Services

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Our Servies :

  • Feasibility assessment & planning
  • Site evaluation
  • Investigator identification
  • Study start up activities
  • Site management
  • Protocol specific study team training
  • Investigator training
  • Ethics committee submission & approval
  • Independent ethics committee
  • Clinical trial budget and contract preparation
  • Coordination between sites and sponsor / CRO
  • Experienced clinical trial coordinators
  • Assistance with query resolution
  • Internal monitoring & audit
  • GCP training
  • Protocol Development
  • Medical Writing
  • BA/BE study set up and design
  • Academic training
  • Trial Identification

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Patient Recruitment

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A Clinical Trial volunteers have the satisfaction of helping find new treatments, cures and preventions for disease and improve the standard of people suffering form varying medical abnormalities universally.

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FAQ Management Service

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What is the clinical study?

The clinical study or the clinical research is trial project which involve patients with specific health conditions and healthy volunteers that helps the doctor for the proper evaluation of potential new drug. As a matter of benefit the specific health conditioned patients undergo free of cost unavailable treatment, and healthy participants receive financial incentives for there inconvenience. All the participants involved in the trial will be given full health check up. Followed by regular monitoring from our panel of medical experts in the medication period and for some duration later too .

What is the purpose of being involved in a clinical trial?

Participation in the clinical trial not only adds to the fact of great contribution to the advance discovery of new medication but also gives the patient to try the opportunity to go through the treatment in a leading health care facility before they are available by their doctor. There could be some good reasons for you to participate, and there may be some draw back which you needed to be aware. In some cases, there may be no approved treatment for your condition, and the only possibility of finding an effective one is through a trial.

Who is eligible to participate in trial?

Criteria for participation may be medical or social, and may include any or all of the following: age, gender, race, diagnosis, the type and stage of a disease, previous treatment history, other medical conditions. In clinical research there is a specific guideline which is named as inclusion/exclusion criteria where the inclusion criteria are the factors which states whom to participate in the trial and exclusion criteria is person prohibited in the trial. Before joining the study the participants are properly screened for its qualification to the study.

What if I want to move out of the trial in between?

Yes, certainly you can move out of the trial at any point of time. Letting know about withdrawal to your doctor or research team with your reason for stepping out of the study.

Being a participant of the trial what I have to go through?

During the participation in the clinical trial process as the number of steps will be followed firstly you will go through health check up, and then detailed instructions will be given to you, monitored cautiously all participants throughout the trial, stay in touch after the trial gets over.

How far is clinical research safe?

As mentioned in the approved protocol a drug might appear quite promising, but its benefits may as yet be unproven. Other trial drugs may be near FDA approval, and doctors may already know most of the risks and benefits. If you participate in the trial you need to undergo extra process of testing but it is only for reassurance by the investigators that the trial subject is safe.

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The principal investigator (PI) has the potential to create the foundation of a strong, positively focused clinical trial. It is crucial that PIs have a clear understanding of expectations with regard to accelerated enrollment and their part in achieving this. By setting goals and standards with the PI and managing expectations, the required results can be achieved.
Investigator Registration Questionnaire Please completes the attached Investigator Registration Questionnaire and Investigator Data Protection Consent Form and return to us scan copy by email only.

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