We provide clinical research personnel and support services to the pharmaceutical, biotechnology and medical device industry. We offer fast, flexible and tailored solutions to our clients with the key advantage of true cost effectiveness.
MKS Research has experience and also pool of potential investigators in many therapeutic fields:
Our team consists of highly qualified CRAs with medical, life science or scientific background who receive continuously further training and education. They conduct ongoing on-site clinical monitoring throughout the trial to make sure that it is conducted, recorded and reported in accordance with the study protocol, ICH GCP and applicable regulatory requirements.
Our CRAs make sure that the reporting guidelines for Adverse Events and Serious Adverse Events are strictly adhered to.
Prior to the study close-out, CRA ensures a timely resolution of data queries prior to the database lock, final study drug accountability and IMP return or destruction.
The site is closed after a thorough review of Investigator Site File is performed to contain all relevant documentation, assessment of regulatory documents, collection of appropriate close-out documents, appropriate archival of trial documentation is ensured.