Divyajivan Healthcare Research Center Surat
The Research mission of divyajivan healthcare research center is to undertake and promote excellence in clinical research & to foster and support patient care and treatment.
Overview & Special Features
Overview & Special Features
At our center, Pharma-sponsored, Government Sponsored,Investigator-initiated & Academic research projects provide the foundation for the research activities. These projects are complemented by multicenter controlled clinical trials & Research training programs.
Special Features:
- Experience & GCP trained research investigators assisted by a dedicated & full-time GCP & NDCT-2019 Rules trained Research team.
- Spacious working area with facilities. For storage, Audit & archival of research related activities.
- Updated SOPs in accordance with national and international regulations.
late phase studies
Our Facility Information
Our Facility Information For Late Phase Studies:
- Dedicated Research Center for Late Phase Studies(Phase II-IV)
- 10000 square foot clinic area
- Trained CRC with 10 seated CRC Room & Monitoring Room
- EC Room and EC Conferance Room with onsite EC Archival Facility
- 24/7 Medical Emergency Service available
- 8 OPD Room for Various Speciality
- 5 Procedure Room for (2D Echo, USG, ECG, TMT, X-Ray, EEG and Sleep Study)
- Separate Chemotheraphy room with Bio-Safety Cabinet with HEPA Filter
- Dedicated phlebotomist/study nurse/pharmacologists
- -30°& -80° storage facility
- Inhouse Laboratory facilities
- Separate Pharmacy for Late Phase Study
- Separate and Secure onsite Archival Facility
- Separate Waiting Room for Patient
Therapeutic area
Therapeutic area
- Internal Medicine
- NASH & NAFLD
- Infection Disease
- Diabetic
- Pulmonary Medicine
- Oncology
- Hypertension
- Gastroenterology
- Rheumatology
- Metabolic Syndrom
- Neurology
- Ophthalmology
- Dyslipidemia
- Cardiology
- Immunotherapy
- Covid-19 Treatment & Vaccine
- Nephrology
- Cardio Vascular Risk Factor
- Ulcerative-colitis & IBD
- CKD with Anemia
- Endocrinology
institutional ethics committee (iec)
Institutional Ethics Committee
Institutional Ethics Committee is an independent body constituted of medical, non-medical, scientific and non-scientific members whose responsibility is to ensure the protection of the rights, safety and well-being of human subjects involved in the trial by, among other things, reviewing, approving and providing a continuing review of trial protocols and amendments.
Timely reviews and safeguarding of high ethical standards formed the basis of the IEC review process which are essential for clinical research including student research, investigator initiated research and multi-centric multinational research.
downloads
Find Publications
Find Publications
- Aprospective, multi-center, double blind, randomized trial of Saroglitazar 4mg compared to placebo in patients with non-alcoholic steatohepatitis – published in Journal of APASL (Asian Pacific Association for the Study of the Liver
- Outcomes of Desidustat treatment in people with Anemia and Chronic Kidney Disease: A phase 2 study — published in American Journal of Nephrology
- Efficacy and Safety of pegylated interferon alfa-2b in moderate COVID-19: A phase II, randomized controlled open-label study— published in International Journal of Infectious Diseases
rights & responsibilities
Research Patient
Rights of Research Participant:
- Right to voluntary participation in a research study.
- Right to know about institutional Ethics Committee and its responsibilities towards protecting patients rights, safety and well-being involved in a research project and to provide public assurance of that protection.
- Right to information about Research Study in an understandable language.
- Right to informed consent and if necessary audio-video consenting before participation in any Research Study.
- Right to refusal of participation or withdrawal of participation at any point in the study without disclosing any reason.
- Right to receive quality healthcare in a safe, clean environment without discrimination because of race, age, color, religion, nationality, culture, ethnicity, language, disability, sex or manner of payment.
- Right to be treated with dignity, respect and courtesy in a non-judgemental and non-threatening manner.
- Right to information regarding an investigational product, duration of the study, treatment option available as per standard of care, anticipated expenditure, information on medical management of any injury and compensation in case of any study related injury or death or any compensation provided for participation in an understandable language.
- Right to be informed of the risks, benefits, and alternatives of proposed treatment.
- Right to privacy and confidentiality.
- Right to be informed on how to voice a complaint to express concerns, violation of your rights and/or grievance and seek redressal.
- Right to participation in research and innovative therapies.
- Right to consent for diagnostic and therapeutic procedures.
- Right to access clinical records.
- Right to get 24 hours emergency contact details of the Research doctor.
- Right to get contact details of Chairperson and Member of Secretary of institutional Ethics Committee.
Responsibilities of Research Participant:
- To provide correct and complete demographic information including full name, age, address, telephone number and email ID. (If available)
- To be compliant with research protocol and procedures.
- To ask the question when he/she does not understand what the doctors, research study team, or other healthcare team members tell about diagnosis or treatment.
- To inform your research study doctor and research study team, immediately in case of injury or development of any new medical conditions.
- Not to take any medications without the knowledge of the research doctor and research study team.
- To disclose to doctors and research study team if currently part of any other Clinical Trial or had participated in any other Clinical Trial in last one year.
- Provide complete and accurate information about your health including your previous medical history, and all the medications that you are presently taking including alternative treatments like Ayurveda, Homoeopathy, Unani or herbal medications, all records of previous investigations and treatment and of allergic reactions, especially sensitivity to any drug.
- To follow instructions, advice and restrictions regarding treatment plans and visit schedules.
- To treat hospital staff and study team with courtesy.
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Great Dentist if you need your family member to get effectiv immediate assistance, examination , emergency treatment o simple consultation. Thank you.
The Richads,12 Main Road
Great Dentist if you need your family member to get effectiv immediate assistance, examination , emergency treatment o simple consultation. Thank you.
