
A Simple Guide to Medical Device Labeling Requirements
In the rapidly evolving world of healthcare, medical device labeling plays a crucial role in ensuring patient safety and regulatory compliance. At Acenth, working closely

In the rapidly evolving world of healthcare, medical device labeling plays a crucial role in ensuring patient safety and regulatory compliance. At Acenth, working closely

In the evolving landscape of clinical research, decentralized clinical trials (DCTs) are gaining increasing attention, especially among healthcare professionals and doctors who play a crucial

Selecting a reliable Clinical Research Organization (CRO) is a pivotal step for healthcare professionals and doctors involved in in vitro diagnostic (IVD) or medical device

In today’s fast-evolving healthcare landscape, diagnostic tools are advancing to meet the increasing demands for speed, accessibility, and accuracy. Two such categories—Over-the-Counter (OTC) and Point-of-Care

The field of in vitro diagnostics (IVDs) is one of the fastest-evolving sectors in healthcare. With advances in genomics, digital diagnostics, and regulatory science, staying

In the fast-paced and highly regulated world of healthcare, clinicians and procurement specialists must ensure that the medical products they use meet the highest standards

In vitro diagnostics (IVDs) have long played a vital role in modern healthcare, offering the precision and speed needed to detect, monitor, and manage diseases.

Operating from the heart of the life sciences sector, Acenth collaborates with Clinical Research Organization (CRO) professionals to better understand the frameworks that support the

In vitro diagnostics (IVDs) are foundational to modern medicine. From genetic panels and infectious disease assays to cancer biomarkers and routine blood tests, IVDs inform

As medical technologies rapidly evolve, the clinical environment has become more reliant on advanced devices—from robotic surgical tools and implantable monitors to AI-driven diagnostics. For