Dr. Mix Cro

Dr. Mix C.R.O. offers several services related to clinical research activities: 1.Consultancy, selection and training of investigators and research sites. 2.GCP training, Regulatory Training, Site Support, Coaching. 3.Translation and Customization of key regulatory documents. 4.Regulatory: Preparation and Submission of regulatory dossier to obtain the necessary regulatory and legal approvals. 5.Logistical and importing processes, storage of supplies and distribution of research materials. 6.Monitoring Services: We provide monitoring, clinical site management and project management services for Clinical Trials from Phase I to Phase IV and Post Marketing Studies. Pharmacovigilance: Safety Officer Services, toxicology, and drug interactions. At the request of the sponsor, this includes follow-up and reporting of adverse events, serious adverse events and Safety Alert reports or CIOMS to the appropriate regulatory authorities. It also includes the designation of a Safety Officer qualified to do these duties.