This includes ensuring that your SOPs: Are uniformly written with detailed instructions to record routine operations, processes and practices followed within a business organization Contain adequate detail to clearly guide research staff through a particular procedure...
The connection between MVG and our data management/biostatistics partners allow us to provide data management & biostats services to our clients, such as statistical programming, data collection, data management and data integration.
MVG offers what some biopharmaceutical companies call a hybrid model approach to clinical study management that protects the sponsor from an under-performing full service CRO.
They accomplish this in multiple ways–by being flexible to the scope of the project, by using our expertise to guide through the clinical data and by demonstrating the efficacy of the drug and by improving patient safety.
Our knowledgeable and multilingual clinical quality assurance (CQA) auditors are well versed in local, national and international regulations, standards and guidelines.
Development of SOPs (Standard Operating Procedures) Study & site startup activities Documents and Submissions IRB/IEC interaction Contracts & budgets Screening and enrollment Study subject activity throughout the trial Regulatory documents (electronic and...
MVG clinical research associates work closely with your team on protocol and indication training, building strong site relationships and ensuring site compliance.
MVG provides companies alternatives to the large contract research organizations, helping small to medium sized biotechnology and pharmaceutical companies with their clinical development programs.
