About 8 Trademarks found for “CAIDYA”

Computer software, namely, downloadable and web-based accessible computer programs for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials, computer program systems consisting of computer hardware and recorded software systems for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials and program libraries in the nature of electronic databases recorded on a data carrier in the field of pharmaceutical research and development and printed and electronic users manuals for use therewith sold as a unit

Study equipment for clinical trials, namely, patient monitors and patient sensors for monitoring and measuring blood properties and respiratory events, medical instruments to measure blood pressure, cardiac output and other physiological and cardiovascular parameters, medical imaging devices for the brain, and similar medical apparatus for detecting cancer or other specific disease types, for use in clinical trials

Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of pharmaceutical, medical, healthcare, and life sciences companies to assist them with clinical research, clinical trials and applications for drug, biologic and device approval; providing independent review of clinical trials for business purposes; contract research organization (CRO) services, namely, business management in the field of clinical trials, namely, clinical data management

Contract research organization (CRO) services, namely, monitoring of clinical trials for drugs, biologics and devices of pharmaceutical, medical, healthcare, and life sciences companies for quality control purposes, and clinical trial project management in the nature of design and implementation of clinical trials and quality assurance for all major therapeutic areas, in particular gastroenterology, nephrology, urology, and oncology; consulting services in the field of scientific research in the nature of conducting clinical trials in the pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; providing quality assurance services in the field of regulatory submissions to regulatory authorities and government agencies by life sciences companies to ensure validity and accuracy of clinical trials; product development for others, namely, providing implementation services relating to the development and validation of drugs, biologics and medical devices; Software as a service (SaaS) services featuring software for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials; contract research organization (CRO) services, namely, custom technical writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports; contract research organization (CRO) services, namely, custom writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports for submission to regulatory authorities; Inspecting potential sites for hosting clinical trials for quality control purposes

Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of pharmaceutical, medical, healthcare, and life sciences companies to assist them with clinical research, clinical trials and applications for drug, biologic and device approval; providing independent review of clinical trials for business purposes; contract research organization (CRO) services, namely, business management in the field of clinical trials, namely, clinical data management

Contract research organization (CRO) services, namely, monitoring of clinical trials for drugs, biologics and devices of pharmaceutical, medical, healthcare, and life sciences companies for quality control purposes, and clinical trial project management in the nature of design and implementation of clinical trials and quality assurance for all major therapeutic areas, in particular gastroenterology, nephrology, urology, and oncology; consulting services in the field of scientific research in the nature of conducting clinical trials in the pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; providing quality assurance services in the field of regulatory submissions to regulatory authorities and government agencies by life sciences companies to ensure validity and accuracy of clinical trials; product development for others, namely, providing implementation services relating to the development and validation of drugs, biologics and medical devices; Software as a service (SaaS) services featuring software for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials; contract research organization (CRO) services, namely, custom technical writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports; Contract research organization (CRO) services, namely, custom writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports for submission to regulatory authorities; Inspecting potential sites for hosting clinical trials for quality control purposes

Computer software, namely, downloadable and web-based accessible computer programs for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials, computer program systems consisting of computer hardware and recorded software systems for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials and program libraries in the nature of electronic databases recorded on a data carrier in the field of pharmaceutical research and development and printed and electronic users manuals for use therewith sold as a unit

Study equipment for clinical trials, namely, patient monitors and patient sensors for monitoring and measuring blood properties and respiratory events, medical instruments to measure blood pressure, cardiac output and other physiological and cardiovascular parameters, medical imaging devices for the brain, and similar medical apparatus for detecting cancer or other specific disease types, for use in clinical trials

Computer software, namely, downloadable and web-based accessible computer programs for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials, computer program systems consisting of computer hardware and recorded software systems for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials and program libraries in the nature of electronic databases recorded on a data carrier in the field of pharmaceutical research and development and printed and electronic users manuals for use therewith sold as a unit

Study equipment for clinical trials, namely, patient monitors and patient sensors for monitoring and measuring blood properties and respiratory events, medical instruments to measure blood pressure, cardiac output and other physiological and cardiovascular parameters, medical imaging devices for the brain, and similar medical apparatus for detecting cancer or other specific disease types, for use in clinical trials

Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of pharmaceutical, medical, healthcare, and life sciences companies to assist them with clinical research, clinical trials and applications for drug, biologic and device approval; providing independent review of clinical trials for business purposes; contract research organization (CRO) services, namely, business management in the field of clinical trials, namely, clinical data management

Contract research organization (CRO) services, namely, monitoring of clinical trials for drugs, biologics and devices of pharmaceutical, medical, healthcare, and life sciences companies for quality control purposes, and clinical trial project management in the nature of design and implementation of clinical trials and quality assurance for all major therapeutic areas, in particular gastroenterology, nephrology, urology, and oncology; consulting services in the field of scientific research in the nature of conducting clinical trials in the pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; providing quality assurance services in the field of regulatory submissions to regulatory authorities and government agencies by life sciences companies to ensure validity and accuracy of clinical trials; product development for others, namely, providing implementation services relating to the development and validation of drugs, biologics and medical devices; Software as a service (SaaS) services featuring software for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials; contract research organization (CRO) services, namely, custom technical writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports; Contract research organization (CRO) services, namely, custom writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports for submission to regulatory authorities; Inspecting potential sites for hosting clinical trials for quality control purposes

Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of pharmaceutical, medical, healthcare, and life sciences companies to assist them with clinical research, clinical trials and applications for drug, biologic and device approval; providing independent review of clinical trials for business purposes; contract research organization (CRO) services, namely, business management in the field of clinical trials, namely, clinical data management

Contract research organization (CRO) services, namely, monitoring of clinical trials for drugs, biologics and devices of pharmaceutical, medical, healthcare, and life sciences companies for quality control purposes, and clinical trial project management in the nature of design and implementation of clinical trials and quality assurance for all major therapeutic areas, in particular gastroenterology, nephrology, urology, and oncology; consulting services in the field of scientific research in the nature of conducting clinical trials in the pharmaceutical industry, the biotechnology industry and the medical device and diagnostics industries; providing quality assurance services in the field of regulatory submissions to regulatory authorities and government agencies by life sciences companies to ensure validity and accuracy of clinical trials; product development for others, namely, providing implementation services relating to the development and validation of drugs, biologics and medical devices; Software as a service (SaaS) services featuring software for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials; contract research organization (CRO) services, namely, custom technical writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports; Contract research organization (CRO) services, namely, custom writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports for submission to regulatory authorities; Inspecting potential sites for hosting clinical trials for quality control purposes

Computer software, namely, downloadable and web-based accessible computer programs for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials, computer program systems consisting of computer hardware and recorded software systems for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials and program libraries in the nature of electronic databases recorded on a data carrier in the field of pharmaceutical research and development and printed and electronic users manuals for use therewith sold as a unit

Study equipment for clinical trials, namely, patient monitors and patient sensors for monitoring and measuring blood properties and respiratory events, medical instruments to measure blood pressure, cardiac output and other physiological and cardiovascular parameters, medical imaging devices for the brain, and similar medical apparatus for detecting cancer or other specific disease types, for use in clinical trials