Tmep Consulting

ABOUT US: TEDMED Engineering and Projects was founded as a 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, Open label, and Phase IV / Post Market. At TMEP, we also utilize our years of experience in the industry to provide excellent services to our clients. Our services include Site Monitoring, Clinical Trial Project Management, Regulatory Submission, Quality Data Management, Computer System Validation, Equipment Validation, Process Validation, Product Quality Assurance, Quality Control, QMS Maintenance and Regulatory Compliance Auditing. Our goal is to serve our client needs and request, and 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 also have a team of biotechnology Engineers, we fix, perform preventive maintenance, validate, commission and qualify medical devices. At TMEP Consulting, we specialize in delivering expert project management and regulatory consulting services across the full spectrum of drug and medical device research and development. Our mission is to help life science organizations navigate the complex journey from concept to commercialization with precision, compliance, and confidence.