TEDMED ENGINEERING & PROJECTS

ABOUT US: TEDMED Engineering and Projects was founded in 2011, as an independent consulting firm. We are a contract, consulting, and project to project clinical research and engineering firm. We specialize in both drug and medical device development. We provide clinical trial management and regulatory services. We work with Pharmaceutical, Biotechnology, Hospitals, Clinics, Research sites, CDMO, CMO, CRAMS, CRO and Medical Device companies. Our services include managing all activities of clinical trials from Preclinical development stages, Phase I, II, III, Open label, and Phase IV / Post Market. At TMEP, we utilize our 16 years of experience in the industry to provide excellent services to our clients. We provide Site Monitoring, Clinical Trial Project Management, Regulatory Submission, Quality Data Management, Computer System Validation, GMP Validation, Process Validation, QA, and QC. Our only goal is to serve our client needs and request, to exceed expectation. We coordinate, initiate, plan, execute, and manage the lifecycle of clinical trials safely and efficiently, serving as the main contact between the sponsor, or CRO and other stakeholders throughout the trial. Our services also include FDA Roadmap meeting, Clinical Trial Planning, Site Selection Qualification, Site Initiation, Interim / Routine Monitoring, Data Management, Trial Logistics, and Clinical Research Project Management. We are also biotechnology Engineers, we fix, perform preventive maintenance, validate, commission and qualify medical devices.