Pharmalys have acquired the Good Clinical Laboratory Practice (GCLP) Accreditation scheme from Qualogy 2002 Ltd. and have provided a seamless transition between the two companies. At our latest accreditation audit the Pharmalys team were professional, knowledgeable and friendly. We are proud to continue to be members of the scheme.

H.L. Facility Manager, UCL ECMC GCLP Facility, London, UK

“Pharmalys commitment to high professional standards and quality of work, coupled with the expertise and knowledge of the African health environment, puts Pharmalys at the forefront of clinical trials in the sub-Saharan region.

I, on behalf of my company, look forward to seeing your continued success in the future.”

L. S., Manager of Overseas Medical Affairs, Biotech, China

Pharmalys have provided monitoring and project management services for several of our vaccine clinical trials. I really appreciate Pharmalys’ great deal of experience with clinical trials in sub-Saharan Africa. They are a hugely valuable source of advice on many matters. They are our eyes and ears at our overseas trial sites, and I feel confident that with Pharmalys’ oversight, our trial sites are working to the highest standard and that any issues or challenges are resolved quickly.

S.W., Clinical Trials Project Manager, University of Oxford

We received some great feedback on the GCP training and I wanted to pass this on to you. How personable and friendly you were, plus the sessions were delivered well with good interaction.

F.H., Clinical Consultant

“I notice the promotion of Assane and Alimatou whose professionalism had impressed us during the prior clinical study, these all speak volumes about the talent and potential within Pharmalys.

It is inspiring to see an organization such as Pharmalys celebrates the achievements of its people and the importance of collaboration with customers. I am confident that with such an approach, Pharmalys will continue to thrive and make a significant impact in the clinical research industry.”

L. S., Manager of Overseas Medical Affairs, Biotech, China

“We are impressed with your company’s reputation for providing high-quality services and believe that your expertise and experience aligns well with our project requirements.”

Associate Director, Clinical, Australian biopharma

Working with Pharmalys has been a real pleasure. They are highly diligent, extremely knowledgeable and have made running our clinical trial in the UK very easy. Certainly, for any other EU studies that I may be working on in the future, Pharmalys will be the first CRO that I will approach.

C. B., Senior Clinical Manager, Biopharma USA

I have worked with Marieme and the Pharmalys team for the last 18 months on multiple submissions for clinical trials for medical devices in Europe and monitoring services for clinical trials. I found them to be extremely thorough, very professional with high working standards and at the same time very patient and pleasant to work with.

Y. M. CEO, Orbix Medical

Pharmalys provides excellent support in a timely manner. No query is too small to be dealt with and all are responded to in a short time frame. Staff are always knowledgeable, polite and easily contacted.

Dr Y. L., Principal Investigator, Ireland