RLM

Administrative management of regulatory submission, namely, assisting others in preparing and filing applications for new pharmaceuticals with governmental regulatory bodies; business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval

Scientific and technological services, namely, scientific research in the field of medicine and pharmaceuticals; research and development in the pharmaceutical and biotechnology fields; technical research in the field of pharmaceutical studies; evaluation and analysis of technical, chemical, clinical and preclinical data for scientific and research purposes in the context of certification and product testing for authorization procedures; scientific and technological consultancy in the context of authorization procedures

Regulatory compliance consulting in the pharmaceutical, biotech and medical device industries; legal consulting services with regard to assistance with marketing authorization procedures in the field of new medical and pharmaceutical product approval; regulatory compliance consulting in the field of prescription drug sampling