The importance of patient payment services in clinical trials
In the field of clinical trials, the proper management of participant payments and compensation is a crucial factor in ensuring transparency and ethical research practices. In Europe, regulations set strict standards to protect patient privacy and ensure that compensation does not unduly influence a participant’s decision to take part in a study.
The crucial role of CROs in ensuring compliance with Clinical Trial Regulations: safeguarding safety and efficacy
Contract Research Organizations (CROs) play a crucial role in ensuring compliance with clinical trial regulations. Beyond ensuring that studies adhere to current regulatory frameworks, CROs also guarantee the safety and efficacy of the treatments under investigation. Learn how CROs contribute to the quality and success of clinical trials and why they are essential for companies seeking clinical research services.
Gene Therapies: Revolutionizing Disease Treatment
Gene therapies represent one of the most significant advances in modern medicine. These innovative techniques allow for the modification of genes within a patient’s cells to treat or prevent diseases, directly addressing the underlying causes of genetic conditions.
The importance of the Trial Master File (TMF) in Clinical Trials: ensuring integrity and regulatory compliance
The Trial Master File (TMF) is an essential component in the management of clinical trials, as it ensures the integrity of data and regulatory compliance of all clinical research. This master file contains all the necessary documentation to evaluate the conduct of the trial and the quality of the data generated, ensuring that Good Clinical Practices (GCP) and international regulations are followed
Sermes CRO obtains CIR Certification granted by the French Government to boost R&D for French companies
At Sermes CRO, we have obtained the certification for the research tax credit, Crédit d’Impôt Recherche (CIR), granted by the Ministry of Higher Education, Research, and Innovation of France.
Recruitment of patients for clinical trials: the importance of thinking about the patient from the start
Recruiting patients to participate in clinical trials can be a complex and costly process for clinical research promoters. However, considering their needs, emotional situation, scientific understanding, and many other factors is key to achieving high participation from the outset of the research.
The gut microbiota and its impact on human health
The gut microbiota is the collection of microorganisms that inhabit our intestines. These microorganisms play a crucial role in our health, influencing digestive processes, the immune system, and mental health. Therefore, it is critical to conduct clinical research on the microbiota to develop effective treatments.
Sermes CRO obtains ISO 9001 and ISO 27001 quality certificates
The nature of our operations – offering clinical research services and solutions – makes obtaining these certificates particularly relevant for our company.
Keys to effective clinical trial monitoring
Clinical trial monitoring is essential for maintaining the quality and integrity of data. In this article, we delve into the keys to effective monitoring and explore how decentralized trials can benefit pharmaceutical and biotechnology companies
Only 6 months left for the transition of all Clinical Trials to CTIS
The deadline for transitioning clinical trials to CTIS ends on January 30, 2025. Studies continuing beyond this date must comply with the Clinical Trials Regulation (CTR), replacing the old CTD. At Sermes CRO, we join the EMA’s effort to communicate this imminent change to clinical trial sponsors in Europe