PLEIAD DEVICES LIMITED

PLEIAD

Training services in human healthcare regulatory affairs, Training services in human healthcare product development planning and project management, and training services in clinical research in the fields of medical devices, pharmaceuticals and biologics;

PLEIAD

Medical and scientific research, namely, conducting clinical trials; technical medical writing for others; providing quality assurance services in the medical device, pharmaceutical and biologic products fields; product development in the field of human healthcare; Conducting research and clinical trials relating to medical devices and pharmaceuticals and diagnostics in the field of ophthalmology;

PLEIAD

Providing technical consulting services and information management services, namely, clinical data and regulatory submission management to medical device, combination product, and ophthalmic product manufacturers to assist them with clinical research, clinical trials and applications for drug, medical diagnostic equipment, and medical device approval; computerized database management and data processing services; business consulting and management in the field of clinical trials, namely, management and compilation of computerized databases in the field of clinical trials for business purposes; statistical analysis and reporting services for business purposes; regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies;

PLEIAD

The mark consists of the word mark PLEIAD with an atom design component above and dots below.;Color is not claimed as a feature of the mark.;Providing technical consulting services and information management services, namely, clinical data and regulatory submission management to medical device, combination product, and ophthalmic product manufacturers to assist them with clinical research, clinical trials and applications for drug, medical diagnostic equipment, and medical device approval; computerized database management and data processing services; business consulting and management in the field of clinical trials, namely, management and compilation of computerized databases in the field of clinical trials for business purposes; statistical analysis and reporting services for business purposes; regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies;