Trials Can Be challenging.

  • 37% of sites fall short of meeting enrollment targets.

  • Over 94% of trials face delays exceeding one month.

  • Sponsors incur losses of $0.5M to $8M daily during trial delays.

  • Dropout rates above 40% jeopardize result validity.

  • Insufficient diversity compromises result generalizability.

There are solution for you.

Our Success KPIs

  • Ethics Committee Approval in 60 Days – 95% Success Rate

  • Site Activation (90 days from the site selection) – 100%

  • Dropout rates <3%.

  • 100% Compliance in Timely AE/SAE Reporting
  • Training compliance – 100%

  • DBL (60 days after LPLV) – 87%

IN-DEPTH
THERAPEUTIC EXPERTISE

Accessible medical and scientific experts improve research quality, reduce sponsor oversight, and enhance outcomes.

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Infectious Disease & Biothreats

Malaria, Tuberculosis, HIV/AIDS, Emerging pathogens - COVID-19, Ebola, Lassa fever, NTDs

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Cardiovascular & Metabolic

Hypertension, Cardiovascular disorders, Diabetes, Obesity, Thyroid disorders and Dyslipidemia

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Hematology & Oncology

Sickle cell, Anemia, Breast cancer, Lymphoma, Prostate, Sarcoma, Cervical cancer, HIV-related malignancies

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Speciality Medicine

Asthma, COPD, Reproductive health, Mental health, Rheumatology, Pain management,

WE’RE HERE TO SERVE YOU

Be assured we prioritize your compliance with GCP, regulatory guidelines, and project schedule while strategically minimizing any potential risks.

Patient Recruitment

Tap into 40+ High-Enrolling Research Sites with Known Patients

Site management and Clinical monitoring

Clinical Monitoring

Highest Quality Data Review and Effective Interaction With Sites

Clinical project management

Project Management

efficient coordination and proactive issue resolution, for on-time, on budget trial

Clinical Regulatory Services

Regulatory Services

bring clarity to compliance, ensuring smoother market access and quicker product launches.

Drug safety and pharmacovigilance

Safety Management

We ensure your trial participants' well-being and regulatory compliance

Site management

Site Management

We optimize site performance and compliance ensuring faster and quality results.

Quality management

Quality Assurance

We support Quality oversight and FDA Audits and Inspection Readiness for your total peace of mind

Quality management

Data Management

Deliver interim and final analysis for faster decision-making, enhancing trial success

Patient Recruitment

Harness 40+ High Enrolling Sites

Site management and Clinical monitoring

Clinical Monitoring

Establish compliance with FDA’s ICH E6

Clinical project management

Project Management

On-time, budget and highest quality

Clinical Regulatory Services

Regulatory Services

Increased Confidence and Peace of Mind

Drug safety and pharmacovigilance

Safety Management

Managed and Minimized Safety Risks

Site management

Site Management

Safely, Ethically and Compliant Studies

Quality management

Quality Assurance

FDA Audits and Inspection Readiness

WE’VE GOT YOU COVERED

We’re Already There.
We’ve Got Wide Geographic Footprint, Phase and Therapeutic Experience To Scale As Your Project Scope and Demand Fluctuates.

Sub-saharan africa CRO

WE’VE GOT YOU COVERED

Accelerate enrollment and gain market entry advantage with access to 1000+ high-enrolling hospitals with databases of a known diverse pool of patient volunteers.

Geographic foot print in Africa

EXPERIENCE THE POWER
OF ACE RESEARCH PARTNERSHIP

THE BENEFIT OF PROVEN TRACK RECORD AND SUCCESSES THAT GETS YOU THE PATIENTS YOU NEED, ON TIME, AT A REASONABLE PRICE, AND PROVIDES QUALITY DATA AND ANALYSIS

Meeting and exceeding your expectations is our goal, and our KPIs reflect our dedication to achieving the highest standards in every aspect of our services.

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3 Easy Steps

To get your product to market, faster

  • Schedule A Meeting

  • Receive A Detailed Proposal
  • Execute With Confidence
SCHEDULE A MEETING