The success of a clinical trial largely depends on the proper documentation of each and every event of the trial. A number of essential documents are required to be maintained for evaluation of the conduct of the trial as well as the quality of the data produced. It is important to note that all the documents produced should be compliant with the recently updated guidelines and regulations.
WorkSure® aims in providing pharmaceutical and medical device companies, a complete, accurate, concise, timed, dated and extensive documentation for smooth conduct and management of clinical trials. We at WorkSure® support in planning, performing and communicating research through preparation of various clinical, regulatory and educational documents viz. Protocol, CRF, Investigator brochure, ICF & other trial related document preparation, editing and reviewing documents prepared by sponsors, preparation of Standard Operating Procedure (SOP), developing quality assurance and quality control (QA/QC) plan, clinical study reports, abstracts and publication writing, poster/presentations for conferences, systematic reviews as well as Meta-analysis for submission in peer-reviewed journals. The staff of WorkSure® associated with medical affairs and clinical research is trained, experienced and well-versed with the medical terms and is capable of filling the void of inadequacies in documentation.
Read more at http://www.worksure.org/clinical-trials-extensive-documentation-pharmaceutical-companies/
No comments:
New comments are not allowed.