Medpoint, LLC

MEDPOINT

MED POINT;Consulting services in the field of medical product approval for commercial purposes; Medical personnel recruitment services and consultation related thereto; Business consultation in the field of medical device, biotechnology, and pharmaceuticals, by providing on-site specialty human resource solutions for medical device, biotechnology, and pharmaceutical companies needing to satisfy state, federal and international standards and regulations. Training and educating medical staffs regarding state, federal and international standards and regulations effecting the development, design and sales of medical devices, biotechnologies and pharmaceuticals. Preparing curriculum regarding state, federal and international standards and regulations effecting the development, design and sales of medical devices, biotechnologies and pharmaceuticals. Conducting audits for companies in the medical device, biotechnology, and pharmaceutical industries to ensure organizations stay current with industry best practices in quality assurance, regulatory affairs, and clinical affairs. Developing clinical best-practices and building quality management systems for companies seeking certification under International Organization for Standardization. Working with companies to build agile regulatory affairs programs to address current regulatory requirements and those subsequently promulgated. Working with companies to build effective auditing programs to ensure regulatory compliance, licensing and registration. Developing clinical strategies and protocols for companies in the medical device, biotechnology and pharmaceuticals industries. Recruiting and placing personnel for companies in the medical device, biotechnology and pharmaceuticals industries. Providing companies in the medical device, biotechnology and pharmaceuticals industries with technical problem solving solutions and systems.; 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; Business management consulting, strategic planning and business advisory services provided to medical device, biotechnology, and pharmaceutical industries.; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for medical device approval;

MEDPOINT

The mark consists of the word medpoint in lower-case with a series of five solid red circles in an arch beginning on the top left of the o in the word medpoint and increasing in size from left to right with the final circle becoming the dot over the i in the word medpoint.;MED POINT;The color(s) black, white and red is/are claimed as a feature of the mark.;Business management consulting and advisory services for the medical device, biotechnology, and pharmaceutical industry; Consulting services in the field of medical product approval for commercial purposes; Medical personnel recruitment services and consultation related thereto; 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; Business management consulting, strategic planning and business advisory services provided to medical device, biotechnology, and pharmaceutical companies, by providing on-site specialty human resource solutions for medical device, biotechnology, and pharmaceutical companies needing to satisfy state, federal and international standards and regulations. Training and educating medical staffs regarding state, federal and international standards and regulations effecting the development, design and sales of medical devices, biotechnologies and pharmaceuticals. Preparing curriculum regarding state, federal and international standards and regulations effecting the development, design and sales of medical devices, biotechnologies and pharmaceuticals. Conducting audits for companies in the medical device, biotechnology, and pharmaceutical industries to ensure organizations stay current with industry best practices in quality assurance, regulatory affairs, and clinical affairs. Developing clinical best-practices and building quality management systems for companies seeking certification under International Organization for Standardization. Working with companies to build agile regulatory affairs programs to address current regulatory requirements and those subsequently promulgated. Working with companies to build effective auditing programs to ensure regulatory compliance, licensing and registration. Developing clinical strategies and protocols for companies in the medical device, biotechnology and pharmaceuticals industries. Recruiting and placing personnel for companies in the medical device, biotechnology and pharmaceuticals industries. Providing companies in the medical device, biotechnology and pharmaceuticals industries with technical problem solving solutions and systems.; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for medical device approval;