Recent advances in AI, including machine learning, natural language processing, and deep learning models, are transforming ...

It was imperative for a large European CMO that produces multiple biologic drugs to select the right product quality and ...

Managing an electronic trial master file (eTMF) is a complex and labor-intensive effort. Centralize and streamline your clinical activities with MasterControl eTMF software systems. Administering a ...

Review the implementation of a holistic Contamination Control Strategy (CCS). Discover four key considerations for assessing ...

Gain insight into three areas that have been key in ensuring a robust contamination control strategy to help ensure ...

Article 16 of the European Union’s Medical Device Regulation and In Vitro Diagnostic Regulation specifically address the obligations of importers and distributors who engage in relabeling and ...

In the medical device industry, the stakes of an FDA inspection are high. Non-compliance can lead to delayed market access, product recalls, or regulatory actions that can jeopardize a company’s ...

The rapid evolution of telehealth is transforming how patients access — and physicians provide — care, a shift accelerated by policy changes adopted during the COVID-19 pandemic. The announcement in ...

The updated requirements for post-market surveillance (PMS) under the EU Medical Device Regulation (MDR), EU In Vitro Diagnostics Regulation (IVDR), and the U.K.'s forthcoming Statutory Instrument (SI ...

Qosina offers a wide selection of clamps and clips for all your prototyping and production requirements. From pinch clamps to intricate flow regulators, Qosina provides product solutions for flow ...

In the area of micro molding, where precision and efficiency are critical, the role of vertical integration assumes fundamental importance. Accumold, a market-leading micro molding innovator has long ...