Oxebridge Quality Resources International is a leader in management system implementation, with offices in North and South America. Since 1999, Oxebridge has provided rapid implementations of ISO 9001, AS9100 and more, using a proprietary approach that does not rely on boilerplate documents. An advocate for standards users, Oxebridge fights for improved ISO standards content, strict adherence to certification and accreditation rules by registrars and accreditation bodies, and for a stronger voice of users within the standards development process. Contact us today to see how Oxebridge can help your organization Be Excellent.

The foundation of a world class organization is based upon a well defined Quality Management System (QMS); a set of processes, procedures and activities that is used to direct, control and monitor an organizations effectiveness and efficiency while providing for continually improving the organization's performance. A well define QMS considers not just the organization implementing it, but also considers the needs of it's customers and suppliers ensuing continuity throughout the supply chain. Today's management system standards call for a process based management approach. For some companies, this can be a daunting task. Advanced Quality Resources can help in identifying primary and supporting processes needed for a complete and effective Quality Management System that adds value. ISO 9001, AS9100, AS9115 (Software Supplement to AS9100), AS9120 & AS9003 are standards that were developed to enhance customer satisfaction as good business practices. They are not prescriptive in that they do not dictate the means in which an organization implements their requirements. An ISO/AS certification affords customers confidence in the ability of their suppliers to consistently deliver products that are conforming to requirements, safe and delivered on schedule. This often results in preferred supplier status for certified suppliers.

Integrity Trials, LLC assists clinical research professionals by providing a vast number of services to enhance the productivity and operations of conducting clinical trials. These services include business developement, site selection, site initiation, staffing, training, site set up, site quality management, Investigator recruitment, in-house monitoring/Phase II-IV, auditing, audit preparation, creating corrective action plans, risk management assessments, suggestions for operational improvement, creation and revision of SOP's, etc. Integrity has over 20 years experiene in the medical field, with 11 of those being in clinical research industry. With a heart to serve and committment for excellence, Integrity's goal is to see your business succeed and enhance your productivity. This goal will not only enhance your business, but provide a genuine reputation that sponsors will know and appreciate. If you are a physician who is new to the industry and would like information about clinical research, we would be glad to sit down with you for a free consultation to discuss the possibility of participating in this exciting and rewarding business opportunity. If you're a physician who is already participating in clinical trials, and you could benefit from our vast number of services, please give us a call. We would be happy to assist you in any way we can.

Quality Innovations conducts consulting to implement or maintain your quality system to meet ISO 9001, ISO 14001, TS 16949, AS 9100, OHSAS 18001. We will customize a system for you provide training and consulting. We also perform contract internal audits to save time and money to ensure you get the most out of your system.

Advanced Biomedical Consulting, LLC is a member of the ABC family of companies, a group of companies known for providing both cost-effective and extremely high quality products and services. ABC provides a wide range of consulting services to industries associated with the manufacturing and distribution of Food and Drug Administration (FDA) regulated products. With a diversified workforce made up of published technical and regulatory experts in the pharmaceutical, medical device/diagnostic, biopharmaceutical, cosmetic, food/seafood, and animal feed industries, ABC can provide cost effective solutions to nearly all issues encountered in FDA regulated industries. Click here to see a list of current and recent ABC projects.

Founded in 2005, Quality Edge provides, R&D Quality Assurance, Medical Device Engineering Quality Assurance, Manufacturing Quality Assurance and Compliance and technical consulting services to clients around the world. • GMP and QSR (21 CFR Parts 820, 210, 211,58,56 and 11) • ISO 13485:2016 • ISO 9001:2015 • ISO 17025 • ISO 14644 (1 to 8) • Medical Devices Directive (European Council Directive 93/42/EEC) • EU Guidelines to Good Manufacturing Practices, Medicinal Products for Human and Veterinary Use • Canadian Medical Device Regulations • Japan's Pharmaceutical Affairs Law (JPAL)