For volunteers

You can contribute to change people’s lives! Imagine what it’s like to know that you’ve been involved in the development of an improved human drug. Thanks to your participation and contribution to the study, a drug was registered and helped tens, thousands or millions of people in the fight against their problems. Being part of socially responsible community that helps people fight diseases and save their lives is what it means to participate in clinical research.
If you would like to know if there are any treatments in clinical trials that might help you, contact your physician.

If you have any further questions on participation in clinical trials and payment methods, please contact the Principal Investigator:
Name: Zhakish Aizhan Nyshanbekovna
Address: Republic of Kazakhstan, Almaty region, Ili district, Energy rural district, Otegen Batyr settlement,
Industrial zone No. 200 A
Tel: +7 777 805 1116/+7 705 170 8825
Fax: +7 727 379 4258
E-mail: pv@consultingasia.kz

Information for volunteers
Requirements
• Healthy volunteer according to the results of all laboratory and instrumental studies
• Age from 18 to 49 years old
• Absence of allergic reactions
• Absence of alcohol and/or drug addiction
• Negative pregnancy test (for female volunteers)
• Agreeing to use double barrier methods of contraception (e.g. condoms with spermicides)
The order of conducting clinical trials of the first phase and bioequivalence
• Join Whatsapp or Instagram and get the latest and most up-to-date information on volunteer recruitment
• Register on the website or call the contact person
• Visit the screening center on the day of the screening
• The presence of an identity card

Screening
• Familiarization with informed consent (contains full information about the upcoming clinical trial)
• Signing an informed consent form with the research physician
• Medical examination, measurement of height, weight
• Laboratory tests (clinical blood test, urinalysis, biochemical blood test, blood test for HIV, syphilis, viral hepatitis B and C)
• Alcohol test
• Urine test for drug and drug abuse
• Pregnancy test (for female volunteers)
• Instrumental studies (ECG)
Based on the screening results, the research physician makes a conclusion on the basis of which the volunteer is allowed or not allowed to the study.

Research Procedures
• Hospitalization at the center on the day before taking the drug from 8.00 a.m. on the day according to the study schedule
• Medical examination
• If necessary, laboratory and instrumental studies, tests for alcohol, drug and drug abuse, pregnancy (for female volunteers)
• Taking the drug (most often carried out from 08-09.00)
• Blood donation for bioequivalence studies of drugs (the first blood sampling is carried out before taking the drug, the time of subsequent sampling corresponds to the study plan)

Completion of the study and payment
• Payment is made immediately on the last day of participation in the study
• The amount of payments is agreed before the start of the study

Volunteer rights
• Choice to participate or not participate in clinical trials
• The opportunity to ask the researcher all the questions of interest, get answers and have enough time to make a decision
• Obtaining all information of interest regarding the study, study drug and the state of own health in full and in an accessible form
• Privacy of personal data
• Constant medical supervision throughout the study providing the necessary qualified medical care if necessary
• Compensation for harm caused by participation in a clinical trial (if any)