Dot Compliance

APRIL 17, 2025

ISO 13485: A Medical Device-Specific Standard ISO 13485 is a specialized standard tailored to the unique requirements of the medical device industry. Good Laboratory Practices (GLP): A Quality Assurance Framework GLP is a set of principles and guidelines that govern the conduct of laboratory studies.

Regulatory Compliance 52

Regulatory Compliance Compliance FDA Medical Device Industry 52

HIT Consultant

JANUARY 31, 2024

What You Should Know: – ECRI , an independent healthcare safety organization, has released its annual Top 10 Health Technology Hazards list for 2024 , highlighting critical safety concerns for healthcare providers and the medical device industry. packaging) included with each product.

Medical Device Industry 98

Medical Device Industry Ransomware FDA Public Health 98

HIT Consultant

AUGUST 21, 2023

According to our own research and data, there is roughly $58 billion in available patient funding, including drug manufacturer copay assistance, foundation grants, government plans, free drug programs, and living expense support. He brings more than a decade of experience in the medical device industry to the company.

Medical Device Industry 98

Medical Device Industry Patient Satisfaction Hospitals Governance 98

Healthcare IT Today

APRIL 13, 2023

Virtonomy’s digital twin technology can help enhance medical device design in a virtual patient setting, accelerating development timelines and reducing costs, risk, and regulatory barriers. Virtonomy is reinventing how medical devices are safely and quickly brought to patients.”

Medical Device Industry 90

Medical Device Industry Governance 90

Healthcare IT Today

FEBRUARY 15, 2024

Tim Bowe, CEO at Full Spectrum Within the healthcare and medical device industries (as well as virtually every other one), focus on incorporating AI into product suites has been a major focus. As artificial intelligence becomes increasingly integral to healthcare, the urgency to integrate ethical governance cannot be overstated.

Medical Device Industry 126

Medical Device Industry Medicaid Medicaid Nurses 126

Dot Compliance

JUNE 16, 2022

Patients and medical professionals have justifiably high expectations for their devices’ safety, quality, and efficacy. Government regulators have been doing their best to ensure that patients receive the safest and most efficient device possible. What is a medical device QMS?

FDA 52

FDA Regulatory Compliance Compliance Governance 52

HIT Consultant

JUNE 12, 2024

Additionally, localized production enables more flexible scaling of capacity to meet demand variations and ensures compliance with regulations governing transportation and distribution.

Medical Device Industry 45

Medical Device Industry Governance Compliance 45