CTIS: a milestone in European clinical research
“The implementation of CTIS is a crucial step towards a more efficient and competitive clinical research ecosystem in Europe, benefiting both researchers and patients.”
The potential of exosomes in regenerative medicine
Regenerative medicine has made significant strides in recent decades, and one of the most promising discoveries in this field is exosomes. These tiny extracellular vesicles are revolutionizing the way we understand and treat tissue and organ repair.
How CROs facilitate the implementation of clinical trials: from planning to execution
CROs (Contract Research Organizations) play an essential role in the implementation and execution of clinical trials. From initial planning to final execution, they ensure that each stage of the process is carried out efficiently and in accordance with regulations.
Data anonymization in clinical trials
Health data are particularly sensitive personal data. Therefore, protecting the personal data of participants in clinical trials is essential, not only for legal reasons but also in ethical terms. The anonymization of these data guarantees the privacy and security of the information, allows compliance with current regulations, and promotes ethics in research.
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.