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Clinical Research

We conduct clinical trials across various therapeutic areas and phases, upholding the highest standards of efficiency and ethical integrity in clinical research throughout Africa.

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Pharmacovigilance

We offer robust pharmacovigilance systems to rigorously monitor the safety profiles of medical products.

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Regulatory Affairs

We streamline the regulatory processes across African countries, providing comprehensive support to ensure compliance and smooth project execution.

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We are a leading CRO that puts patients and clients at the forefront; let us partner to achieve greater success together.

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Who We Are

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THESYL is a leading Contract Research Organization (CRO) providing top-tier Clinical Research, Pharmacovigilance, and Regulatory services across Africa. Incorporated in the Sweden, with offices in Sweden and in Rwanda, our company is deeply rooted in a mission to advance health research and innovation by facilitating the development and delivery of safe and effective life-saving medicines and therapies that address the unique healthcare challenges of the African continent.

What We Do

Clinical Research

We conduct and manage clinical trials in various therapeutic areas and across all phases, handling everything from study design and protocol development to site selection, patient recruitment, data management, and regulatory compliance. Our aim is to ensure quality, efficient and ethical clinical research across Africa.

Pharmacovigilance

Our team offers robust pharmacovigilance solutions to monitor the safety profile of medical products throughout their lifecycle by identifying, detecting, and evaluating adverse events to ensure timely risk management and regulatory reporting."

Regulatory Affairs

We navigate the complex regulatory landscape of African countries, providing comprehensive regulatory support, including dossier preparation and submission, and interactions with local regulatory authorities. We guide sponsors and bio-pharma companies through the registration process, ensuring compliance with all local, regional, and international regulations.

How We Do It

THESYL employs a multidisciplinary team of professionals with extensive experience in pharmaceutical research, healthcare regulation, and project management. By leveraging our deep understanding of local healthcare ecosystems and global best practices, we deliver high-quality, efficient, and cost-effective solutions to our clients. Our collaborative approach fosters strong partnerships with stakeholders across the healthcare industry, enabling us to drive innovation and accelerate the development of life-saving therapies.

Why Choose Us?

Deeply Rooted Expertise

Our team boasts a unique blend of African experience and global best practices. We understand the intricacies of African healthcare systems and navigate regulatory hurdles with confidence.

Seamless Clinical Development

From meticulous trial design and strategic site selection to efficient data management, we ensure your clinical research runs smoothly across diverse African regions.

Unwavering Patient Safety

Our robust pharmacovigilance programs prioritize patient safety. We actively monitor drug safety and ensure safe and effective medical products throughout their lifecycle.

Regulatory Navigation

Deciphering the complexities of African regulations is our specialty. We guide you through the registration process, ensuring compliance at every stage.

Tailored Approach

We offer a highly customizable approach, tailoring our services to meet the specific needs and challenges of each project. Our flexibility ensures that we can adapt to the unique requirements of different studies, delivering personalized and effective solutions.

Innovative Technological Solutions

Leveraging cutting-edge technology, we streamline the clinical trial process with advanced electronic data capture (EDC) systems, real-time reporting tools, and robust data analytics, ensuring accuracy, efficiency, and actionable insights.

What People Say
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Placide Sophroni UWINGENEYE
Managing Director of USOPHARMA Ltd

“We began collaborating with THESYL on drug market registration projects, and their expertise has been instrumental in guiding us through the process. Their regulatory services have proven invaluable, and we look forward to extending this partnership into our upcoming pharmacovigilance initiatives. With THESYL's dedication to excellence, we are confident that future projects will continue to meet the highest standards of safety and compliance”

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Dr. Sylvestre NTILIVAMUNDA
Director of CMSF

“At Clinique Medicale Sainte Famille (CMSF), we are deeply appreciative of the invaluable support provided by THESYL in preparing us for future clinical trials. Their expert guidance on regulatory requirements, robust quality assurance processes, and strategic planning services have been instrumental in ensuring our compliance, readiness, and alignment with our research goals. With their assistance, we are well-prepared to advance medical research and patient care”

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