Domains targeting keyword medical device regulatory consulting

Qserve: Global Partner for Medical Device Regulatory Consulting, Clinical Trials and Quality. Need regulatory advice, support or training? Contact us

Validation Consulting Inc. offers compliance, regulatory, risk management, and validation services for biotech, pharma, and medical device industries.

Regulatory guidance, validation strategies, technology reviews, expert consulting, training, references, current news, upcoming events and our blog.

Consulting firm specializing in medical device & pharmaceutical regulatory compliance, FDA inspection readiness, quality engineering & validation projects

800.325.8252 |We're a world leader in medical device testing, equipment, services and consulting. Core products & services centered around stent testing, heart valve testing, acute particulate stent testing, fatigue to fracture stent testing, and coated durability device testing. Over 30 years of experience.

Greenleaf Health is a leading FDA regulatory consulting firm that provides strategic guidance to pharmaceutical and medical device companies developing and manufacturing innovative solutions to pressing global public health challenges.

Regulatory and Quality Solutions (R&Q) provides industry-leading regulatory and quality consulting and engineering services to medical device companies.

ENV Services, Inc nationwide leader in calibration, validation, HPV (hydrogen peroxide vapor) decontamination and certification of clean air equipment and environments

The world's leading FDA consultants, providing expert regulatory affairs, compliance, biotech, medical device and pharmaceutical consulting services.

Intertech Engineering Associates assists medical device manufacturers bring their products to the market. We help you design, develop and validate your devices; assist in managing projects and build our clients internal expertise. Intertech understands the regulatory challenges our clients face, and our time tested development and validation processes anticipate and address problems inexpensively on the planning board.

Providing expert microbiology, rapid microbiological method, GMP, contamination control, regulatory, product quality and expert witness consulting solutions for the pharmaceutical, biopharmaceutical and medical device industries.

Hospitals, healthcare systems, and medical device manufacturers post-market surveillance, adverse event analytics, compliance reporting and consulting to improve patient safety and reduce risks and costs of quality events across the supply chain. Addresses FDA, CDRH and EU MDR regulatory requirements for quality management systems and recalls

Compass Biotech is a full service consulting firm offering strategic and technical expertise to our clients in the pharmaceutical, medical device, diagnostic and biotech industries.

Validation & FDA Compliance Solutions

MCRA, Musculoskeletal Clinical Regulatory Advisors, MCRA Consultants, MCRA Advisors, Medical Device Consulting, Medical Device Advisory Services, Biologics Advisory Services, Medical Device Regulatory Services, Biologics Regulatory Services, Medical Device Reimbursement Services, Biologics Reimbursement Services, Medical Device Clinical Services, Biologics Clinical Services, Medical Device CRO, Medical Device Clinical Affairs, Biologics Clinical Affairs, Medical Device QA Services, Biologics QA Services, Medical Device Quality Assurance, Biologics Quality Assurance, Medical Device International Regulatory, Medical Device IP, Medical Device Intellectual Property.

Emergo: medical device consultants for QA/RA, device registration, clinical trials, reimbursement and distribution consulting. Offices worldwide.

MethodSense provides quality management and regulatory compliance consulting to medical device companies throughout product commercialization.

Integra System is a wireless and medical device strategic consulting firm. We have decades of experience working with medical device companies and end clients helping them navigate through engineering design, FCC and regulatory testing, and product branding.

Medical device expert with engineering, science and business degrees, 20 years experience in the medical, pharmaceutical, biotech, and regulatory industry who worked with companies around the world.

Japan MDC plays a cooperative role in work on such revisions with the government, PMDA and related industrial groups. As a result, it is in a strong position to help applicants navigate the related registration process of regulatory approval for medical device and offer a variety of support services for product registration with its expert knowledge of trends in Japan's regulatory environment.

Thema: regulatory affairs and quality consulting for medical devices and IVDDs, international registrations, GMP, QTA, distribution. Agencies worldwide.

FDA consulting for the medical device industry, pharmaceutical industry and food industry for US and EU FDA quality assurance and regulatory compliance

Validant delivers end-to-end Quality, Compliance, and Regulatory consulting service for healthcare companies around the world that is simply best in class.