Clinipace, Inc.

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

Consultation in the field of publishing and issuing scientific papers in relation to conducting clinical trials, regulatory affairs, drug development, manufacturing compliance and validation, advanced technology, clinical benchmarking and clinical performance improvement in the field of international health and in the pharmaceutical, biotechnology, and medical device industries; Computer software, namely, downloadable 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 users manuals for use therewith sold as a unit; clinical trial logistical services, namely, delivering clinical trial kits to sites, delivering wearable devices to patients and/or site locations; Providing user access to a global computer network in connection with clinical trials and drug development; Provision of access to a computer network in connection with clinical trials and drug development; Real estate site selection namely, building inspecting in the course of building construction of potential sites for hosting clinical trials; Medical and pharmaceutical consultation; Study equipment for clinical trials, namely, patient monitors and patient sensors for monitoring and measuring health 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 medical apparatus for detecting cancer, for use in clinical trials; 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; 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; regulatory compliance consulting in the pharmaceutical, medical, healthcare, and life sciences fields; 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 the FDA by life sciences companies to ensure validity and accuracy; 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

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; 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; regulatory compliance consulting in the pharmaceutical, medical, healthcare, and life sciences fields; 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 the FDA by life sciences companies to ensure validity and accuracy; 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

Consultation in the field of publishing and issuing scientific papers in relation to conducting clinical trials, regulatory affairs, drug development, manufacturing compliance and validation, advanced technology, clinical benchmarking and clinical performance improvement in the field of international health and in the pharmaceutical, biotechnology, and medical device industries; Computer software, namely, downloadable computer programs and downloadable computer programs provided via a website 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; clinical trial logistical services, namely, delivering clinical trial kits to sites, delivering wearable devices to patients and/or site locations; Providing user access to a global computer network in connection with clinical trials and drug development; Provision of access to a computer network in connection with clinical trials and drug development; Real estate site selection namely, building inspecting in the course of building construction of potential sites for hosting clinical trials; Medical and pharmaceutical consultation; 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 symptoms related to specific disease types in the fields of cardiology, cell and genes, gastroenterology, infectious diseases, nephrology, neurology, oncology, rare diseases, respiratory, and women's health, for use in clinical trials; Inspecting potential sites for hosting clinical trials for quality control purposes; providing temporary use of web-based computer software programs for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials

Consultation in the field of publishing and issuing scientific papers in relation to conducting clinical trials, regulatory affairs, drug development, manufacturing compliance and validation, advanced technology, clinical benchmarking and clinical performance improvement in the field of international health and in the pharmaceutical, biotechnology, and medical device industries; Computer software, namely, downloadable computer programs and downloadable computer programs provided via a website 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; Clinical trial logistical services, namely, delivering clinical trial kits to sites, delivering wearable devices to patients and/or site locations; Providing user access to a global computer network in connection with clinical trials and drug development; Provision of access to a computer network in connection with clinical trials and drug development; Real estate site selection namely, building inspecting in the course of building construction of potential sites for hosting clinical trials; Medical and pharmaceutical consultation; 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 symptoms related to specific disease types in the fields of cardiology, cell and genes, gastroenterology, infectious diseases, nephrology, neurology, oncology, rare diseases, respiratory, and women's health, for use in clinical trials; Inspecting potential sites for hosting clinical trials for quality control purposes; providing temporary use of web-based computer software programs for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials

Consultation in the field of publishing and issuing scientific papers in relation to conducting clinical trials, regulatory affairs, drug development, manufacturing compliance and validation, advanced technology, clinical benchmarking and clinical performance improvement in the field of international health and in the pharmaceutical, biotechnology, and medical device industries; Computer software, namely, downloadable computer programs and downloadable computer programs provided via a website 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; Clinical trial logistical services, namely, delivering clinical trial kits to sites, delivering wearable devices to patients and/or site locations; Providing user access to a global computer network in connection with clinical trials and drug development; Provision of access to a computer network in connection with clinical trials and drug development; Real estate site selection namely, building inspecting in the course of building construction of potential sites for hosting clinical trials; Medical and pharmaceutical consultation; 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 symptoms related to specific disease types in the fields of cardiology, cell and genes, gastroenterology, infectious diseases, nephrology, neurology, oncology, rare diseases, respiratory, and women's health, for use in clinical trials; Inspecting potential sites for hosting clinical trials for quality control purposes; providing temporary use of web-based computer software programs for accessing, collecting, managing, tracking, analyzing, and reporting data and information on 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 the FDA by life sciences companies to ensure validity and accuracy; 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 | 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; regulatory compliance consulting in the pharmaceutical, medical, healthcare, and life sciences fields

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 the FDA by life sciences companies to ensure validity and accuracy; 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 | 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; regulatory compliance consulting in the pharmaceutical, medical, healthcare, and life sciences fields

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 the FDA by life sciences companies to ensure validity and accuracy; 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 | 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; regulatory compliance consulting in the pharmaceutical, medical, healthcare, and life sciences fields

Consultation in the field of publishing and issuing scientific papers in relation to conducting clinical trials, regulatory affairs, drug development, manufacturing compliance and validation, advanced technology, clinical benchmarking and clinical performance improvement in the field of international health and in the pharmaceutical, biotechnology, and medical device industries; Computer software, namely, downloadable computer programs and downloadable computer programs provided via a website 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; clinical trial logistical services, namely, delivering clinical trial kits to sites, delivering wearable devices to patients and/or site locations; Providing user access to a global computer network in connection with clinical trials and drug development; Provision of access to a computer network in connection with clinical trials and drug development; Real estate site selection namely, building inspecting in the course of building construction of potential sites for hosting clinical trials; Medical and pharmaceutical consultation; 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 symptoms related to specific disease types in the fields of cardiology, cell and genes, gastroenterology, infectious diseases, nephrology, neurology, oncology, rare diseases, respiratory, and women's health, for use in clinical trials; Inspecting potential sites for hosting clinical trials for quality control purposes; providing temporary use of web-based computer software programs for accessing, collecting, managing, tracking, analyzing, and reporting data and information on clinical trials

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 writing for others for non-advertising purposes in the nature of medical writing of clinical study protocols and reports; 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; 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; regulatory compliance consulting in the pharmaceutical, medical, healthcare, and life sciences fields; 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 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 the FDA by life sciences companies to ensure validity and accuracy; product development for others, namely, providing implementation services relating to the development and validation of drugs, biologics and medical devices

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; 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; 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; regulatory compliance consulting in the pharmaceutical, medical, healthcare, and life sciences fields; 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 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 the FDA by life sciences companies to ensure validity and accuracy; product development for others, namely, providing implementation services relating to the development and validation of drugs, biologics and medical devices