Clinical Trail Unit

Welcome to Haripur International Hosptial

Clinical Trials Unit

Need for Clinical Research

Haripur International Hospital Clinical Trial Unit is a DRAP-approved facility committed to conducting high-quality Phase II, III & IV clinical trials. We ensure strict compliance with both local and international regulatory standards, following the principles of Good Clinical Practice (GCP).

Our team brings together therapeutic expertise, innovative end-to-end solutions, and global research capabilities to design and deliver successful trials with precision and care.

We excel in efficient patient recruitment, exceptional retention, reliable high-quality clinical trial data, and streamlined sponsor oversight.

Discover how our Clinical Trial Unit can be tailored to meet your study requirements, timelines, and budget.

We Invite

International Clinical Trials (Phase II–IV)

We Offer

Advanced Healthcare You Can Trust

We Focus

Precision, Safety & Performance

Advancing Research Improving Outcomes

What Sets Us Apart

Haripur International Hospital Clinical Trial Unit partners with biopharmaceutical and biotechnology companies, international and local Contract Research Organizations (CROs), and Site Management Organizations (SMOs) to address patient recruitment and site management challenges. Our expertise ensures efficient recruitment strategies and superior site performance, leading to reliable, high-quality clinical trial outcomes.

How Our Trials Work

At our state-of-the-art, purpose-built Clinical Trial Unit, we provide end-to-end support for clinical research through a streamlined process that prioritizes compliance, safety, and efficiency.

Consent Room

A private, confidential space where the Principal Investigator (PI) and study team conduct informed consent in full compliance with ICH-GCP guidelines.

Vitals & Screening

Standardized assessments to determine eligibility, carried out under the supervision of the PI and study team.

IP Administration

Safe and accurate administration of the investigational product, overseen by the PI and trained study staff.

IP Storage & Randomization

Secure and compliant handling, storage, and randomization of investigational products, with full PI accountability.

Observation Room

Dedicated space for post-dosing monitoring, ensuring participant safety under the close supervision of the PI and study team.

Sample Storage

Controlled storage conditions for biological samples, maintained with oversight from the PI to ensure integrity and compliance.

Archiving Room

Secure facility for the retention and management of essential study records, safeguarded under the PI’s responsibility.

About Us

Discover Advanced Clinical Research at Haripur International Hospital

Medical Specialitie

Experience Breakthrough Clinical Trials at Haripur International Hospital

Collaborations

Advancing Healthcare Through International Partnerships

Pharmacovigilance

Introducing the Minds Shaping Innovative Research

Work With Us

Have Questions? Speak With Our Clinical Research Team

Our Gallery

Frequently Ask Questions

Participating in a clinical trial offers several meaningful benefits:

  • Early Access to Innovative Treatments – Gain access to promising therapies before they become widely available.

  • Personalized Medical Care – Receive close monitoring and support from a dedicated team of healthcare professionals.

  • Contribute to Medical Progress – Play an important role in advancing research that may improve healthcare for countless others.

  • Compensation & Support – Many studies offer financial compensation for your time, and some may provide health insurance coverage during participation.

By joining a clinical trial, you take an active role in your health journey while helping researchers develop safer and more effective treatments for the future.

While clinical trials are conducted under strict safety standards, it’s important to understand the potential risks:

  • Possible Side Effects – Treatments or study procedures may cause mild to severe side effects.

  • Uncertain Effectiveness – The investigational treatment may not provide the expected benefits.

  • Unexpected Complications – In rare cases, unforeseen health issues may arise.

Your safety is always the highest priority. Every clinical trial undergoes rigorous ethical and scientific review to minimize risks and ensure your well-being is carefully protected throughout the study.

Each clinical trial has defined eligibility criteria to ensure participant safety and reliable study results. These may include:

  • Age and Gender

  • Type and Stage of Your Condition

  • Medical History and Previous Treatments

  • Overall Health Status

To find out if a trial is right for you, consult your doctor or contact the Clinical Trial Unit team at Haripur International Hospital. Our specialists will review your information, assess eligibility, and guide you through the next steps if a suitable trial is available.

In most clinical trials, there is no cost to you as a participant. The investigational treatment, related tests, and study procedures are typically covered by the sponsor.

Many studies also provide compensation for your time, travel, and participation.

Our goal is to ensure that joining a clinical trial does not create a financial burden, so you can focus fully on your health while contributing to important medical research.

As a participant, you are protected by several key rights to ensure your safety, privacy, and freedom of choice:

  • Informed Decision – You will receive clear details about the trial, including potential risks and benefits, before you decide to take part.

  • Voluntary Participation – Joining a trial is your choice, and you may withdraw at any time without affecting your routine medical care.

  • Privacy & Confidentiality – Your personal and medical information will remain secure and protected throughout the study.

  • Medical Care & Support – If you experience side effects, you will receive appropriate medical care and, where applicable, compensation as outlined in the trial policy.

These rights are designed to safeguard your well-being and ensure you are respected at every stage of the clinical trial.

If you’re interested in participating in a clinical trial or believe you may be eligible:

  • Consult Your Doctor – Discuss whether a clinical trial may be a good option for your health needs.

  • Contact Our Clinical Trial Unit – Our team will guide you through available opportunities, answer your questions, and support you at every step to ensure a safe and comfortable experience.

📧 Email: clinicalresearch@haripurinternational.com
📞 Phone: +92 333 4442076

By joining a clinical trial, you play an active role in your healthcare while helping advance medical research for the future.

Partner with DRAP APPROVED SITE

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