Our key focus is on delivering innovative solutions to our clients that accelerate drug development, reduce time and costs, and ensure high quality results. Since our establishment in 2004, we have fine-tuned our business model to reflect validated best practices from the most highly regulated venues, which we have carefully tailored to suit local environments.
Cromos Pharma’s mission is to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
Rapid enrollment is supported by our “NO PATIENTS – NO PAYMENT” program which means that Sponsors pay only for enrolled patients and not for dormant, non-recruiting sites.
By choosing Cromos Pharma you get an unwavering guarantee that your project will be handled by the “A-Team”. Our clinical research professionals, 95% are MDs or have their PhDs, will stay with you for the duration of your study, have a true local expertise, and are fully invested in the success of your clinical trial.
Our experienced feasibility team will swiftly prepare a detailed capability/feasibility report and will propose the optimal path forward, including country/venue strategy and site-selection within the recommended venues.
By analyzing protocol design, study population, sites’ motivation to enroll, subjects’ barriers to participation, and competing clinical programs, we developed a dynamic approach to identifying and resolving any issues related to subject recruitment and retention.
If your study is behind schedule or encounters difficulties with patient recruitment, Cromos Pharma will provide a comprehensive and collaborative rescue plan to ensure your investments yield a return and that your study meets its timelines and milestones.
Our team of experts have years of experience working with international regulatory agencies on the most complicated protocols. In the ex-US territories, favorable regulatory environment coupled with our in-depth local knowledge of submission guidelines and algorithms assures that your study is initiated as quickly as possible.
The welfare of our patients is our utmost priority. We are fully compliant with the ICH-GCP and make sure that the patients in our studies are well-informed and have a direct line of communication to both the investigators and to our research team.
Our Quality Management System is built upon Quality by Design principles that include integrated planning, quality agreements tailored to the project, real-time project risk-based analysis, data analytics-driven targeted monitoring, and customer-focused project optimization.
Over the past 20 years Cromos Pharma has conducted over 350+ clinical trials in a vast range of therapeutic indications. The graphs below represent the last 3 years of this experience.
*Other: Pediatrics, Dermatology / Infectious diseases, Vaccines, Gynecology / Surgery, Trauma / Surgery, General Medicine, Hepatology, Trauma, Nephrology, Musculoskeletal, Hematology, Allergology, Surgery / Anesthesia, Obstetrics / Gynecology, Nutrition
I would like to recognize Cromos Pharma's team for its outstanding work and want to express my sincere gratitude. Thank you for your help during the FDA inspection. You have displayed admirable characteristics which led to a more trusting and effective partnership between Cromos Pharma and our company. As we work together effectively, we are showing great benefit to our studies and most importantly to our patients. I hope to continue a close and successful working relationship with you.
I want to thank you for your work on the XXXX study. It is very important to our top management that we have met the timelines. I am sure that in many respects it is a credit to Helen S. I was touched by Helen’s personal approach, her deep knowledge of all study phases, her desire to explain and answer the questions at any time. Due to Helen’s work with the PIs we managed to collect almost perfectly filled CRFs, to respond quickly to all queries and lock database and obtain a statistical report on time. Special thanks from the finance department for the transparent and duly provided financial documents.
For the time we have worked together, I notice the efforts to respond to any of Sponsor’s requests in a timely manner and with a real good sense of priority/efficiency that allow our Project Management Team to know how the XXXX study is moving forward. Therefore, it is a real pleasure to receive your packages (documents, reports, trainings records) in headquarters. All is perfectly filed, documents are well scanned, named and I do not miss any time with such administrative tasks.
I have been impressed with the proactivity and the desire to get things done that has been shown by each one of the Cromos Pharma team with whom I have interacted with. My experience with Cromos Pharma has certainly been positive, especially taking into account the study on which we are currently working together is a really complicated one.
