by milena henderson | Jun 16, 2026 | Clinical Operations, Quality & Business Excellence
In clinical research, maintaining accurate, complete and accessible documentation is essential to ensuring precision, compliance and effective oversight throughout a study. As clinical trials continue to become more complex, the need for efficient document management...
by milena henderson | Mar 10, 2026 | Clinical Operations, Health research
The recent suspension of a proposed hepatitis B birth-dose vaccine trial in Guinea-Bissau has prompted critical reflection across the global research community. At Pharmalys, we believe this moment represents both a warning and an opportunity: a reminder that Africa...
by Veronique Ropion | Apr 23, 2025 | Clinical Operations
Obtaining clinical informed consent is both an ethical and legal requirement before invasive medical or surgical procedures. In research, informed consent must be sought and secured before enrolling a participant in a study. The concept of informed consent is founded...
by Veronique Ropion | Mar 4, 2025 | Clinical Operations
My journey with Pharmalys began in 2019 when I collaborated directly with the company from the sponsor side. I was eager to continue contributing my expertise to clinical research (CR), particularly managing and leading clinical trials (CT) in Africa. In April 2021,...
by Veronique Ropion | Oct 22, 2024 | Clinical Operations
The clinical trial landscape has undergone significant changes since the concept of trials was first introduced, with notable shifts in the social, ethical, and regulatory environments worldwide. The Clinical Trial Landscape Is Evolving Today, there is a broader...
by Veronique Ropion | Sep 17, 2024 | Clinical Operations
Pharmalys Ltd is a regional Contract Research Organisation (CRO) that has seen significant growth over the past three years. Headquartered in Europe with regional offices in Dakar, Pharmalys supports sponsors around the world in conducting safe and high-quality...
