Healthworld Hospitals is Durgapur's first and single largest Hospitals having experience of conducting the clinical trials over last 04 years with certified and experienced Clinical Research Coordinators and Principal Investigators. HWH conducts phase I, II, III and IV clinical trials, of which 80% are global multi-centric trials.

HWH is a NABH-accredited multispecialty hospital with 300 beds, with 88 Senior Physicians. It is a centre for excellence in the field of Cardiology (Drug/Device), Paediatric Cardiology, Pulmonology, Gynaecology, Urology, Endocrinology, Gastroenterology, Neurology, Nephrology, General medicine, Ophthalmology & Dermatology.

Our institute has its own department of laboratory, which is NABL accredited. It comprises clinical biochemistry, haematology, microbiology, histopathology and cytology.

Ethics Committee :

Healthworld Hospitals have its own institutional ethics committee, named "Healthworld Hospitals Institutional Ethics Committee” It is registered under Central Drugs Standard Control Organization [CDSCO] with registration number ECR/1404/Inst/WB/2020. It is also registered under Department of Health Research [DHR] This committee shall evaluate, scrutinize and monitor all clinical research. The role of the ethics committees is “to protect and maintain the dignity, rights, safety and well-being of all research participants”.

Important Information :

  • IEC Meeting Dates: Last Saturday of every month (exact date & day may change)
  • Project Submission Deadline: 3 weeks prior to date of meeting.
  • Applications received after the deadline will be taken up in the next meeting
  • Clearance from IEC is necessary even for projects that have been cleared by other institutions/agencies
  • The documents should be submitted to: A complete set of documents should also be emailed to ethicshwh@gmail.com or Contact 8170052905, Incomplete applications will be returned.

Collaboration Partners :

We have collaborations with various sponsors, CROs and SMOs for carrying out various clinical research studies like Johnson & Johnson, Bayer, Abbott, Novo Nordisk, Intas pharma, Glenmark, IQVIA, JSS research/GD Genesis, clicebo, Lambda research

How do we works ?

1. Clinical Trial Conduct :

  • Institutional Review Board (IRB): The study protocol is submitted to an Institutional Review Board (IRB) for ethical approval. Hospitals have IRBs that review and approve research protocols to ensure they adhere to ethical guidelines and protect the rights and safety of participants.

2. Patient Recruitment and Screening :

  • Eligibility criteria : Researchers define specific criteria for potential participants, such as age, diagnosis, and medical history.
  • Informed Consent : Researchers obtain informed consent from each participant, explaining the study's purpose, potential risks and benefits, and their right to withdraw at any time.
  • Protocol Adherence : Researchers follow a detailed protocol that outlines the study design, procedures, data collection methods, and safety monitoring.
  • Data Collection: Data is collected through various methods, such as medical records, questionnaires, physical exams, and laboratory tests.
  • Safety Monitoring: Researchers closely monitor participants for adverse events and side effects, taking immediate action if necessary.

3. Additional Considerations :

  • Patient safety Throughout the research process, patient safety is the top priority.
  • Data privacy and confidentiality Strict measures are taken to protect the privacy and confidentiality of patient information.
  • Regulatory compliance : Clinical research must adhere to all relevant regulatory guidelines and standards.

Our Accreditations

Contact Us :

    8170052760 clinicalresearch@hwhos.com