Clinical trials in Pune
Manipal Hospitals conducts regulated clinical trials in Pune across diverse therapeutic areas, following strict protocols to ensure participant safety and scientific accuracy. Each study involves screening, informed consent, baseline assessments, intervention delivery, and structured follow-up. Research teams explain eligibility, study goals, and safety measures clearly before enrolment. Participants receive investigational treatments in a controlled environment along with standard medical oversight. Digital systems enable accurate data capture, safety reporting, and continuous monitoring to maintain study integrity and protect participant welfare.
Hospital Locations
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Kharadi - Pune
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Baner - Pune
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Clinic Dhanori - Pune
How It Works
Clinical trials at Manipal Hospitals, Pune, begin with an initial screening. Research investigators evaluate medical history, diagnostic reports, and study-specific criteria to determine participant eligibility. Study procedures, requirements, and potential risks are discussed thoroughly during the informed consent process.
Baseline assessments follow, including physical examinations, laboratory tests, imaging, and measurements required to establish pre-intervention status. Once eligibility is confirmed, participants are enrolled and assigned to study groups in accordance with the protocol. During the intervention phase, investigational drugs, devices, or procedures are administered exactly as per the approved trial design. All dosing, timing, and adherence parameters are recorded. Participants return for scheduled monitoring visits for safety checks, laboratory evaluations, symptom review, and treatment assessments.
Throughout the study, safety oversight is maintained through continuous monitoring, adverse-event reporting, and ethics committee review. At study completion, participants undergo final evaluations, and long-term follow-up may be scheduled based on study requirements. With robust research systems, trained investigators, and protocol-driven processes, Manipal Hospitals ensures safe and effective participation in drug trials in Pune.
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Request a CallbackBenefits
Choosing to participate in a clinical trial at Manipal Hospitals, Pune, offers the following benefits:
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Access to investigational therapies within a regulated research environment
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Continuous safety monitoring by trained research and clinical teams
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Standard medical oversight was maintained throughout participation
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Contribution to scientific progress and development of future treatments
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Full regulatory compliance, ensuring participant rights, privacy, and safety
What to Expect
Before Participation
Patients undergo a detailed screening that includes medical history review, diagnostic assessments, and confirmation of eligibility. The informed consent process explains the study’s purpose, procedures, possible risks, and expectations.
Preparation Phase
Participants receive instructions about baseline visits, fasting requirements, medication restrictions, or lifestyle considerations needed for accurate assessment.
During the Trial
Participants attend scheduled clinical evaluations, laboratory tests, and intervention sessions. Continuous monitoring identifies side effects, tracks progress, and ensures adherence to protocol guidelines. Any concerns or new symptoms are reported immediately to the research team. Research staff also guide participants on maintaining consistency with study-related routines to ensure accurate results.
Study Completion
Final evaluations assess treatment response and safety outcomes. Participants receive a closing summary, follow-up recommendations, and guidance on transitioning back to regular medical care.
Why Manipal?
Manipal Hospitals, Pune, is a leading site for medical research in Pune due to its well-established regulatory framework, trained investigators, and dedicated research infrastructure. All clinical studies follow approved protocols, ethics committee oversight, and safety-driven procedures to protect participants throughout the research process.
The hospital offers integrated services, including laboratory diagnostics, pharmacy, imaging, and speciality consultations, allowing participants to complete all assessments on-site without external referrals. Electronic data capture systems ensure accuracy, confidentiality, and compliance with regulatory requirements. Research pharmacy services manage investigational drugs with temperature-controlled storage and secure dispensing.
With coordinated research teams and meticulous documentation practices, Manipal Hospitals, Pune, maintains high standards across every medical study. The hospital ensures that each research activity is conducted ethically, safely, and with full scientific integrity.
Centre of Excellence
The Clinical Research Department at Manipal Hospitals, Pune, oversees all trial-related activities, including protocol implementation, participant screening, informed consent, data collection, and regulatory submissions. The department works closely with ethics committees, clinical teams, and the research pharmacy to ensure adherence to approved protocols. It also manages safety monitoring and accurate reporting across all phases of each clinical study.
Services Offered
Key services provided by the Clinical Research Department at Manipal Hospitals, Pune, include:
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Assistance with protocol development and regulatory documentation
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Participant screening, eligibility verification, and informed consent management
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Investigational product storage and dispensing through the research pharmacy
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Continuous safety monitoring and adverse-event reporting
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Follow-up visits and outcome assessments aligned with study requirements
Facilities & Services
Manipal Hospitals, Pune, provides state-of-the-art facilities, including:
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Dedicated clinical research suites and monitoring rooms
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Secure electronic data capture and storage systems
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Temperature-controlled storage for investigational products
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On-site laboratory and imaging services for efficient assessments
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Experienced research coordinators and clinical monitors ensure protocol compliance
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Participant-friendly environments that support safety and comfort
Frequently Asked Questions
A clinical trial is a regulated research study that tests new treatments, devices, or procedures in humans. Manipal Hospitals, Pune, follows approved protocols, ethics oversight, and structured safety monitoring for all clinical trials.
Eligibility depends on the specific study. Researchers evaluate medical history, diagnostic findings, and protocol-defined criteria to determine whether a participant qualifies. They also ensure that participants understand the study requirements before enrolling.
Benefits of clinical trials may include access to investigational therapies, while risks may involve side effects or unknown outcomes. Each study has safety plans, monitoring schedules, and reporting systems to manage these risks.
Safety is maintained through ethics committee approvals, trained clinical staff, predefined monitoring visits, and emergency procedures. Adverse-event reporting guidelines are also built into every study protocol to ensure thorough oversight.
Yes. All participant data is safeguarded in accordance with strict privacy and regulatory standards. Records are securely stored and accessed only by authorised staff involved in clinical trials in Pune, ensuring complete confidentiality.
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