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Providing clients with a flexible approach to improve cycle times, constrain costs, and reduce risks. Specialising in the planning, management, execution, and analysis of Phase 2-3 clinical trials.
At CRSB’s, our mission is to support the pharmaceutical, biotech, and medical device industries in developing new products and bringing them to market. As a Contract Research Organization, we offer a range of services, including clinical trials management, regulatory affairs, data management, and biostatistics.
Our team of experienced professionals is dedicated to providing high-quality and cost-effective solutions that accelerate the drug development process and improve patient outcomes. By partnering with [Name of CRO], clients can streamline their development programs and achieve their goals faster and more efficiently.
Medical writing and publishing involves the creation of documents and materials related to healthcare products or services. This includes scientific articles, regulatory documents, and marketing materials.
Clinical management encompasses a broad range of activities related to the planning, execution, and oversight of clinical trials. It involves coordinating study timelines, managing resources, and ensuring compliance with regulatory requirements.
The medical device technical file is a collection of documents that demonstrate the safety and performance of a medical device. It includes technical specifications, testing data, and regulatory compliance information.
A quality management system is a set of procedures and processes that are designed to ensure that a company’s products or services consistently meet or exceed customer expectations. In the healthcare industry, quality management systems are critical to ensuring patient safety and regulatory compliance.
Hybrid clinical solutions combine traditional clinical trial approaches with digital technologies and data analytics. They can offer more efficient and effective ways to conduct clinical research while reducing costs and accelerating timelines.
Medical affairs refers to a range of activities related to the medical and scientific aspects of healthcare products or services. It includes activities such as medical education, clinical research, and regulatory affairs.
Regulatory affairs involves the process of ensuring that healthcare products or services comply with regulatory requirements. This includes submitting applications for approval and maintaining compliance with ongoing regulatory requirements.
Biostatistics involves the application of statistical methods to analyze biological and medical data. It plays a critical role in designing and interpreting clinical studies and helps to ensure that study results are accurate and reliable.
Our development experts apply their expertise to make products and treatments accessible to patients through our Site & Patient Solution — whether it’s patient insight for optimised trial design, engagement with patient advocacy groups or customized patient recruitment strategy
Our team of experienced professionals is dedicated to providing high-quality and cost-effective solutions that accelerate the drug development process and improve patient outcomes. By partnering with [Name of CRO], clients can streamline their development programs and achieve their goals faster and more efficiently.
1200+ global pharmacovigilance experts bring together all safety services into a seamless delivery solution.
Our professionals apply their therapeutic, regulatory, and operational expertise to consistently solve the challenges that arise during clinical projects.
We increase predictability in patient recruitment by making it easier for the site and the patient.
At our clinical research organization, we strive to provide comprehensive support for your study needs. Our experienced teams are equipped with the knowledge and skills necessary to navigate complex clinical trials. In addition to our dedicated personnel, we utilize state-of-the-art technologies to streamline data collection and analysis, ensuring efficient and accurate results. Trust us to be your partner throughout your clinical study and beyond.
Providing clients with a flexible approach to improve cycle times, constrain costs, and reduce risks. Specialising in the planning, management, execution, and analysis of Phase 2-3 clinical trials.
Providing clients with a flexible approach to improve cycle times, constrain costs, and reduce risks. Specialising in the planning, management, execution, and analysis of Phase 2-3 clinical trials.