DRAP-Licensed Contract Research Organization in Pakistan

Overview

DRAP Licensing Overview

Minerva Research Solutions is a DRAP-licensed and ISO 9001:2015 certified Contract Research Organization (CRO) based in Pakistan. As a certified CRO, we are now authorized to carry out clinical studies in Pakistan under DRAP clinical trial guidelines.

Our license also authorizes us to apply our U.S.-based expertise in conducting clinical trials, engaging sponsors, and serving as a trusted link between leading healthcare institutions in Pakistan. This allows us to deliver accessible, high-quality, and cost-effective research solutions.

Our DRAP authorization confirms:

Official CRO in Pakistan
Compliance with DRAP’s 2017 guidelines
Proper facility inspections and SOP reviews
License to support local and global trials
Expertise in implementing GCP & ICH standards
Adherence to clinical trial ethics
Reliable systems to deliver clean, reliable data

Partner with Us

Why Choose Minerva Research Solutions?

Conducting clinical trials isn’t a one-size-fits-all process; it takes strategic coordination, local insight, and global standards to do it right. At Minerva Research Solutions, we bring years of U.S.-based experience to Pakistan’s growing clinical research landscape. Now operating as a licensed CRO under DRAP, we’re here to lead the way in delivering high-quality, compliant, and patient-centered trials.

We manage every detail, from clinical trial site setup to recruitment, operations, and data management, with a focus on supporting both international sponsors and local sites. Our diverse expertise, right tools, and people-first approach make us more than just a service provider; we’re a partner in your study success.

Whether you’re launching a new trial or expanding your research footprint, Minerva is ready to move forward with you, as your partner, not just a provider.

FAQs

Frequently Asked Questions

Get answers to commonly asked questions about our DRAP licensing and clinical research services in Pakistan

Why is DRAP-licensed important for clinical trials?

It is important because it demonstrates that clinical trials are conducted under strict regulatory standards and guidelines.

What steps did Minerva take to get DRAP approval?

We underwent through Pakistan DRAP approval process including documents submission, facilities inspection, and proving our team’s skills and expertise.

Can Minerva manage both local and international studies?

Yes, our DRAP license enables us to conduct both local and global clinical trials according to international standards.

How do you maintain data quality and regulatory compliance?

We use structured workflows, quality control systems, and regular audits to deliver accurate data that aligns with regulatory standards.

Which types of clinical trials can you conduct in Pakistan?

We run all trial phases (I-IV) and study types, such as drug trials, observational studies, and bioequivalence tests.

What standards and guidelines do you follow?

We follow DRAP’s Bio-Study Rules 2017, GCP guidelines, ICH standards, and also have ISO 9001:2015 certification.

What services can you provide as a DRAP-licensed CRO?

We offer complete clinical trial management. For example, regulatory submissions, site management, data monitoring, and quality assurance.

Partner with Pakistan’s own CRO, delivering global research standards with local dedication.

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Minerva Research Solutions is Pakistan’s own licensed CRO, delivering DRAP-compliant, full-spectrum clinical trial services with global research standards, operational integrity, and a deep commitment to local and international sponsors.

DRAP-Licensed