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.