MarksMan specializes in providing high-quality end-to-end solution for all your SLR requirements. Our multi-disciplinary team has rich experience in all stages of the SLRs, right from reconstructing SLR objectives to PICOS headings, till preparing SLR report.
We are well-versed in evidence generation following global standards, hunting for evidence from scientific publications, conference proceedings, unpublished clinical trials, theses, white papers, government reports, patents, and various other sources of information.
MarksMan assists in development of health economic models to support reimbursements, health technology assessment (HTA) submissions, and to optimize market access strategies.
We understand that successful market access also depends on real-world evidence and HEOR. Because of our breadth of knowledge, we provide services throughout the product lifecycle to ensure optimal pricing and access.
Medical devices seeking marketing authorization must submit a detailed clinical evaluation report (CER) to the regulators. Our team is experienced with preparing CERs for medical devices in accordance with the relevant guidelines, including MEDDEV 2.7/1