Our Pakistan team builds on US‑proven processes to manage multiple study phase, including site setup, data handling, safety, and final reporting under DRAP rules.
See how our US‑honed contract research organization expertise adapts to Pakistani trials
About Us
Minerva Research Solutions brings years of US trial experience to Pakistan’s growing clinical research landscape. Therefore, we are ready to partner with sponsors, hospitals, universities, and regulators to design, launch, and complete studies under DRAP guidelines. Our integrated services including project management, site support, regulatory affairs, data operations, medical writing, and more, reflect our commitment to quality and compliance.
In every project we combine local insight with global best practices so Pakistani and international sponsors alike can run clinical trials that meet DRAP standards.
Certified by the Drug Regulatory Authority of Pakistan (DRAP)
We hold full DRAP accreditation for clinical trial oversight and employ a systematic approach to ensure consistent quality and compliance. Our team includes Pakistan‑licensed pharmacists, statisticians, and medical monitors; all operating under GCP and ISO 9001:27001 quality systems to ensure trials meet the highest global and local regulations.
Our Pakistan Service Suite
Minerva Research Solutions bring together global best practices and local insight to support every study phase, ensuring DRAP‑compliant consistency, operational efficiency, and reliable results.
- Site Management
- Regulatory & Ethics Submissions
- Patient Recruitment & Retention
- Data Management & Biostatistics
- Pharmacovigilance
- Monitoring & Quality Assurance
Site Management
We handle site activation and training in line with DRAP guidelines, manage local logistics, and deliver centralized progress reports. Regular visits and targeted support help each site meet enrollment targets and quality standards.
Regulatory & Ethics Submissions
Our regulatory specialists prepare full submission packages for IRB and DRAP review, manage amendment filings, and liaise with authorities. We combine U.S. expertise with local requirements to keep your trial compliant.
Patient Recruitment & Retention
We design and deploy community outreach programs, digital campaigns, and site‑level engagement to identify and retain participants. Our retention strategies include regular check‑ins, feedback loops, and participant support services to maintain enrollment momentum.Â
Data Management & Biostatistics
From eCRF design and database validation to real‑time data cleaning and advanced statistical analysis, we ensure your datasets meet international standards. Interactive dashboards and clear reports empower sponsors to make informed decisions.
Pharmacovigilance
Our safety team captures all adverse events, conducts thorough case assessments, and submits timely E2B reports. We maintain an up‑to‑date safety database, flag potential risks, and advise on risk‑management measures throughout the trial.
Monitoring & Quality Assurance
We conduct on‑site and remote monitoring visits, perform risk‑based QA audits, and review documentation against GCP requirements. Our corrective action plans and staff training sessions keep sites inspection‑ready and uphold trial integrity.
Built for Pakistan, Proven in the USA
Why choose us? Because, at Minerva, we combine global SOPs with the local know‑how, navigating DRAP requirements while maintaining the speed and transparency sponsors expect from a leading contract research organization.
LET’S WORK TOGETHER
Driving Impact Through Collaboration
We partner with local hospitals, academic centers, and CROs to streamline trial operations. By combining community insight with global expertise, we deliver efficient, DRAP‑compliant studies that meet sponsor expectations.
Local Site Partnerships
We work hand in hand with site teams to address logistical challenges, train staff under DRAP guidelines, and maintain open feedback loops that drive enrollment and quality.
Global Compliance Expertise
Our US‑honed regulatory know‑how guides every submission and audit. We bridge local requirements and international standards to keep your trial inspection‑ready.
Technology Integration
We deploy secure eCRF systems, real‑time dashboards, and remote monitoring tools so sponsors and sites have transparent access to study data and metrics.
ABOUT US
OUR PHILOSOPHY
People‑First Approach: Today, Tomorrow, Till the End
We believe trials succeed when sponsors, sites, and participants share clear goals, open dialogue, and mutual respect. Have a look at how our CEO, Dr. Mazhar Jaffry upholds this philosophy:
“I believe that clinical research thrives on trust. We build that through every protocol briefing, site visit, and data review; combining scientific rigor with local engagement to advance patient care here in Pakistan.”
-Dr. Mazhar Jaffry
Every decision we make reflects our commitment to ethical practices, quality results, and the communities we serve in Pakistan and beyond.
Spotlight on Emerging Trends in Pakistan Trials
In Pakistan’s evolving clinical research environment, sponsors and sites are embracing decentralized trials, digital engagement, and advanced data analytics to improve recruitment and retention. Growing patient awareness and clear DRAP guidelines enable innovative designs such as hybrid studies and remote monitoring. At Minerva Research Solutions, we combine our US‑honed expertise with local insights to support your trials in adopting these approaches, enhancing participant experience and accelerating decision making throughout the study lifecycle.
These trends reflect shifts toward participant‑centric care, positioning Pakistan at the forefront of clinical practice.
Let’s Work Together
Our Guiding Principles
Minerva Research Solutions brings global trial management expertise to Pakistan so local sponsors and sites can leverage US‑tested processes and regulatory insights. Our vision, mission, and values guide every partnership and procedure, ensuring ethical integrity, operational excellence, and shared commitment to advancing clinical research quality and trust.
Our Vision
To be recognized across Pakistan and beyond as the leading contract research organization that brings transparent communication, operational excellence, and ethical standards to every phase of study management.
Our Mission
To partner with sponsors, sites, and regulators in Pakistan by providing comprehensive clinical research services rooted in quality, compliance, and local insight shaped by our US experience.
Our Values
We uphold integrity, respect, and accountability in every project. We value close collaboration, diversity, and cultural sensitivity. We commit to transparency and continuous improvement across all trial phases.Â
Why Sponsors Choose to Work with Us
Our CRO offers sponsors grounded advantages, including cost-effective operations, globally aligned expertise, and seamless collaboration that doesn’t cut corners. It’s clinical research with precision, without inflated overheads.
Smarter Budgeting
Conducting trials in Pakistan means lower site and resource costs without compromising on quality or timelines. It’s practical, sustainable, and sponsor friendly.
Globally Compatible
We follow internationally recognized protocols and documentation standards, making your transition from local execution to global submission simple and compliant. Â
Local Access, Global Transparency
Our teams work across time zones with responsiveness and cultural fluency, ensuring clear updates, fast resolutions, and one consistent research experience.
Minerva Research Solutions is dedicated to accelerating your clinical trials through comprehensive
From the Minerva Desk
Stay ahead with articles on Pakistan trial best practices, regulatory shifts, and global CRO innovations.
How Minerva Simplifies Clinical Trials Operations in Pakistan
How Minerva Simplifies Clinical Trials Operations in Pakistan
Why Choose Minerva Research for Clinical Trial Management?
Why Choose Minerva Research for Clinical Trial Management?
Frequently Asked Questions
Have questions about running DRAP‑regulated trials with our contract research organization in Pakistan? Explore the FAQs and their answers below to learn more about us and what we do.
What makes you a reliable contract research organization in Pakistan?
We merge US trial rigor with DRAP license and local expertise for end‑to‑end study management.
How do you handle DRAP submissions?
Our regulatory team prepares, submits, and follows up on all DRAP and IRB applications.
Can you support international sponsors?
Yes, we align Pakistan operations with regulatory and sponsor requirements seamlessly.
Can international sponsors expect the same quality standards from a CRO based in Pakistan?
Absolutely. We follow globally recognized research practices and maintain rigorous internal oversight to ensure sponsors get reliable results and professional coordination at every step.
How do you ensure data integrity?
We use validated eCRFs, real‑time dashboards, and biostatistics checks to catch issues early.
Let’s Connect
Get In Touch
Partner with Pakistan’s own CRO, delivering global research standards with local dedication.
GET STARTED TODAY
