Clinical Trail Unit

Welcome to PMC

Clinical Trials Unit

Need for Clinical Research

Clinical Trials Unit

Premium Medical Complex, Clinical Trials Unit is a DRAP-approved facility dedicated to conducting high-quality Phase II, III & IV clinical trials. We ensure adherence to local and international regulatory requirements and the principles of Good Clinical Practice. 

We combine deep therapeutic expertise, innovative end‑to‑end solutions, and global capabilities to build successful trials with precision and care.

Wedeliver efficient recruitment, excellent patient retention, high-quality clinical trial data, and streamlined sponsor oversight.

Learn more about how our clinical trial unit can adapt to your study requirments , timelines and budget.

We Invite

We Offer

We Focus

Global Clinical Trials (Phase II-IV)

World-Class Health Care

Safety, Quality &Speed

Better Research Better Result

Our Advantage

Premium Medical Complex helps Sponsor from biopharmaceutical & biotechnology companies, International and Local Contract Research Organization (CROs) and Site Management Organizations (SMOs) to overcome patient recruitment and research site challenges to deliver superior patient recruitment performance.

Clinical Trial Unit Workflow

Clinical Trials Unit

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

Consent Room

Confidential space for PI and study team to conduct informed consent per ICH-GCP.

Vitals & Screening

Standardized eligibility assessments under PI and team supervision.

IP Administration

Safe investigational product dosing overseen by PI/study staff.

IP Storage & Randomization

Secure, compliant IP handling with PI accountability.

Observation Room

Post-dosing monitoring by study team under PI supervision.

Sample Storage

Controlled preservation of biological samples with PI oversight.

Archiving Room

Secure retention of study records under PI responsibility

About Us

Explore the Cutting-Edge Clinical Research at PMC

Medical Specialitie

Discover Breakthrough Clinical Trials at PMC

Collaborations

Global Partnerships Advancing Medical Research at PMC

Pharmacovigilance

Meet the Visionaries Behind PMC's Clinical Research Excellence

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Have Questions? Connect With PMC's Research Experts

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Clinical Trials Unit

Frequently Ask Questions

Clinical Trials Unit

Taking part in a clinical trial can provide several advantages:

  • Access to new treatments before they are widely available to the public.

  • Personalized care and close monitoring from a team of healthcare professionals throughout the study.

  • The opportunity to contribute to medical advancements that could help improve healthcare for others in the future.

  • Financial compensation in many studies for your time and participation.

  • Potential health insurance coverage during the trial, depending on the specific study.

By joining a clinical trial, you are not only taking an active role in your own healthcare but also helping researchers find better treatments for others.

Although clinical trials are carefully monitored for safety, there are some risks to consider:

  • Possible side effects from the treatment or procedures involved in the study.

  • The treatment may not provide the expected benefits for your condition.

  • In rare cases, unexpected health complications could occur from the treatment.

Your safety remains the top priority. Every clinical trial goes through strict ethical and scientific reviews before starting to ensure that risks are minimized and your well-being is protected.

Every clinical trial has specific eligibility criteria to determine who can join. These may include:

  • Age and gender

  • Type and stage of your condition

  • Your medical history and any previous treatments

  • Your overall health status

To see if a clinical trial is right for you, talk with your doctor or reach out to the CTU-PMC team. They can help check your eligibility and guide you through the next steps if there’s a suitable trial available for you.

For most clinical trials:

  • There is no cost to participate. The study treatment and required tests are usually covered.

  • You may receive compensation for your time, travel, and participation, depending on the study.

We believe joining a clinical trial should not create a financial burden, allowing you to focus on your health while contributing to medical research.

As a clinical trial participant, you have several important rights:

  • You will receive clear information about the trial, including its potential risks and benefits, before deciding to join.

  • Participation is completely voluntary. You can withdraw from the trial at any time without affecting your regular medical care.

  • Your personal and medical information will remain confidential and protected throughout the study.

  • If you experience side effects from the study treatment, you may receive medical care or compensation according to the trial’s policy.

These rights ensure your safety, privacy, and choice are respected throughout your participation in a clinical trial.

If you’re interested in joining a clinical trial or think you may qualify:

  • Talk to your doctor to see if a trial might be right for you.

  • Reach out to the CTU-PMC team for guidance on available options and to get your questions answered. We will support you through each step to ensure you can join safely and comfortably.

📧  Email: clinical@pmcpk.com
📞  Contact: +92 330 2298777

Your participation can help advance medical research while taking an active role in your health.

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Clinical Trials Unit

Partner with DRAP APPROVED SITE

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