RIMSYS

Regulatory submission management, namely, assisting others in preparing and filing applications for medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated products with governmental regulatory bodies; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for medical device approval; Providing information and news in the field of business, namely, information and news on current events and on economic, legislative, and regulatory developments as it relates to and can impact businesses; and 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; Regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies

Regulatory compliance consulting in the field of medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries; Tracking and monitoring regulatory requirements in the field of medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, cannabis, and other regulated industries for regulatory compliance purposes; Computer software licensing