Federal clean energy incentives are (mostly) gone—but “the glass is more than half full,” according to a new report. The details: 74% of new clean energy capacity and 71% of new clean generation ...

In today’s biopharmaceutical landscape, quality control (QC) microbiology has evolved from its traditional, reactive role in detecting contamination. It now has become an essential pillar in ...

The proposed reforms are intended to make pharmaceutical drugs cheaper, prevent shortages and speed up delivery of new compounds – Copyright AFP/File Louisa ...

A comprehensive contamination control strategy must include a dedicated section addressing personnel-related microbiological and particulate contamination risks introduced into an aseptic process, as ...

As the revised EU GMP Annex 1 continues to reshape sterile manufacturing expectations, pharmaceutical companies across Europe and globally are encountering increasing challenges in the implementation ...

Nottingham, UK - Upperton has submitted its application to the UK Medicines and Healthcare products Regulatory Agency (MHRA) for the approval of its new 7,000 sq. ft sterile manufacturing facility.

Cell therapy manufacturing is uniquely vulnerable to contamination, variability, and operational burden because the product - living cells - is not amenable to terminal sterilization or sterile ...

Innovation and patient safety have always been the cornerstones of the pharmaceutical industry. Today, much of this innovation comes in the form of complex drug formulations and smarter aseptic ...

E-Waste World Expo North America is the continent's premier trade show and conference dedicated to electronics recycling and sustainable e-waste management. This technology-driven event brings ...