Kernel Research and Data Analytics

"Where Every Study Starts with Strategy and Ends with Success"

Kernel is a Contract Research Organization (CRO)

Focused on advancing healthcare in the MENA region through clinical research and public health investigations. We integrates international best practices with local regulatory knowledge, partnering with academic institutions, healthcare professionals, and industry leaders. Kernel provides end-to-end research services, from study design to postmarketing surveillance, aiming to improve patient outcomes through impactful results.

Our Capabilities

Clinical Trials Integration

Real-World Evidence

Public Health & Policy

Our Mission

To drive healthcare innovation through expert, ethical, and efficient clinical research solutions, delivering trusted results that enhance patient care and transform lives.

Our Vision

To drive healthcare innovation through expert, ethical, and efficient clinical research solutions, delivering trusted results that enhance patient care and transform lives.

Our Research Support Services

Medical Writing

Statistical Analysis

Regulatory Affairs Product Registration

Research Design Consultation

Data Collection and Management

Literature Review Services

Kernel, Where Healthcare Solutions Converge with Innovation and Integrity.

Explore the Various Regulatory Services we offer

Pharmaceuticals

Bringing a medical product to market is challenging. We use our specialized expertise to ensure full compliance

Medical Devices

We will help your business Enter the MENA Market of medical devices and equipment.

Cosmetics

Explore our Cosmetics Regulatory Services. We assist brand owners, manufacturers, and distributors.

From Rules to Results

We Make Compliance Your Competitive Edge

Regulatory Pathway Determination

We provide end-to-end support selecting the most effective and efficient regulatory pathway for your product. By analyzing regional regulations, risk levels, and data requirements, our team identifies the optimal route to expedite approvals.

Regulatory Dossier Preparation and Submission

We expertly compile essential product information, from clinical data to manufacturing protocols, presenting it in the required format and structure. We use our agency relationships to expedite reviews and ensure swift MENA approvals.

Labeling Review and Localization

Our team understands that an effective label does more than inform—it builds trust. We ensure that your product labeling resonates with regional consumer bases and complies with local linguistic and regulatory mandates.

Consultation

We deliver specialized regulatory affairs consultation meticulously crafted to navigate the dynamic complexities of healthcare product oversight. We devise bespoke strategies that optimize product registration, expedite approvals, and safeguard ongoing regulatory alignment.

Active Regulation Tracking

Our specialized monitoring services keep you informed about new or updated regulations, policies, and guidelines across MENA jurisdictions. By providing regular intelligence reports and strategic advice, we enable agile adjustments to your product strategies, safeguarding compliance and fueling a competitive edge in rapidly shifting markets.

Post-Market Services

Once your product hits the market, ongoing safety and performance monitoring becomes critical. Our services involve collecting, analyzing, and reporting real-world evidence to detect adverse events swiftly. We help you uphold compliance and sustain long-term consumer trust in the MENA region.