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Medical Device Quality Articles & Analysis

6 articles found

Biopharma PEG Launches New Monodispersed PEGs for Better Drug Delivery

Biopharma PEG Launches New Monodispersed PEGs for Better Drug Delivery

Media Contact: Biopharma PEG 108 Water Street, Suite 4D, Watertown, MA 02472, USA TEL: 1-857-928-2050 / 1-857-366-6766 sales@biochempeg.com About Biopharma PEG: Biopharma PEG is a leading supplier of PEG derivatives, dedicated to supporting the pharmaceutical, biotechnology, and medical device industries with high-quality products that enhance ...

ByBiopharma PEG Scientific Inc


What is a Medical-Grade Welding Gas Mixer?

What is a Medical-Grade Welding Gas Mixer?

Precision is not just a preference but a stringent requirement in medical equipment manufacturing. At the heart of this precision lies the role of medical-grade welding gas mixers, an important component in ensuring high-accuracy welding applications, particularly in environments where consistency and quality cannot be compromised. This blog post defines medical-grade welding gas mixers and ...

ByEnvironics, Inc.


Reliable Ultra-Low Freezers for the Storage of Cancer Biomarkers

Reliable Ultra-Low Freezers for the Storage of Cancer Biomarkers

The use of tumour markers to diagnose, assess prognosis, and select a suitable cancer treatment has become possible due to the development of inexpensive and user-friendly molecular analysis tools such as the polymerase chain reaction (PCR). Maintaining the integrity of biomarkers during their processing and storage is therefore of critical importance to accurately diagnose and give prognosis ...

ByB Medical Systems


Developing Research and Medical Diagnostic Products

Developing Research and Medical Diagnostic Products

From conception to finished commercial product, medical devices requires innovative engineers and product designers, experienced project managers, quality control experts, and substantial regulatory expertise to make that transition a successful one. ...

ByBMP Medical


A Quick Overview of ISO 13485 Requirements for Medical Device Companies

A Quick Overview of ISO 13485 Requirements for Medical Device Companies

It is an undeniable fact that safety and quality are the top-most priority for medical device companies. However, the best-practices to maintain these priorities are defined under ISO 13485. ...

ByQualityze Inc


Why FDA Compliance Needs A Defined CAPA Process.

Why FDA Compliance Needs A Defined CAPA Process.

The medical device industry is worth hundreds of billions of dollars, but companies who take their eye off the ongoing need for quality management could find themselves under an unwelcome federal compliance spotlight. ...

ByEtQ, LLC

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