CLINLOGIX

Printed training materials in the field of clinical trials and life sciences research

Vendor management services for the administration and conduct of clinical trials for others; Business consulting and management in the field of life sciences which may include, clinical trials, namely, clinical data and regulatory submission management on behalf of medical device, diagnostics, and biopharmaceutical and biotechnology companies to assist them with research and development of intellectual property, that may include clinical research, clinical trials and applications for drug approval; Regulatory submission strategy, preparation and management, namely, assisting others in preparing and filing applications for medical devices, diagnostics, biologics, pharmaceuticals interacting with governmental and/or regulatory bodies globally; Regulatory submission management, namely, consulting and assisting others in preparing and filing applications for clinical trials in the field of life sciences with governmental regulatory bodies; Business consulting and management in the field of clinical trials, namely, providing information management services; Services comprising the recording, transcription, composition, compilation and systematization of written communications and recordings, as well as the compilation of mathematical or statistical data

Financial advice, namely, budget planning for life sciences

Arranging professional workshop and training courses; Training for handling scientific instruments and apparatus for research in laboratories

Consulting services for others in the field of design, planning, implementation and project management of clinical trials; Providing medical and scientific research information in the field of pharmaceuticals and clinical trials

Regulatory compliance consulting in the field of clinical trials and life sciences research; Consultation services in the field of the safety needs of commercial and industrial companies; Consulting services in the field of state and federal regulatory compliance requirements for personnel safety; Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research