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What Are Good Manufacturing Practices (GMP)? Good manufacturing practices (GMP) are a system of procedures and controls used to ensure products are consistently produced and meet d...
RNA sequencing combined with nanopore technology and machine learning may streamline GMP quality control testing for mRNA therapeutics within a single workflow...
Duplicate GMP inspections are a major challenge for biopharmaceutical manufacturing companies. The IFPMA urges regulators to rely on audits carried out by peers to minimize the tim...
Scientific breakthroughs are never the result of guesswork; they are the product of rigorous methodology and verified materials. In the study of metabolic health, the use of target...
SHANGHAI, April 20, 2026 /PRNewswire/ -- Mabwell (688062.SH), an innovation-driven biopharmaceutical company with a fully integrated industry chain, announced that its wholly-owned...
The guidance was developed to help manufacturers and laboratories in the design, conduct, evaluation, and reporting of Protein Efficiency Ratio (PER) studies.
In manufacturing, maintaining product quality is essential. Quality departments should be involved throughout the entire process, from engineering to shipping, to ensure high stand...
Gummi World highlights how ingredient sourcing, rigorous certifications, and manufacturing precision define true supplement quality. The post Gummi World Highlights Hidden Quality...
bioMérieux Unveils BIOFIRE SPOTFIRE Molecular Testing Solution for Biopharma Redefining rapid mycoplasma testing Megan Wallin-Kerth Thu, 04/23/2026 - 12:02...
Mukesh Kumar, a SAP Premium Engagement Leader and enterprise transformation strategist, has spent more than two decades designing and delivering large-scale quality, compliance, an...
Company is among the first in China's drug-device combination products sector to obtain this certification, delivering superior solutions to global clientsZero non-conformities dem...
The project leverages AGC Biologics’ global network, having completed cell line development in Copenhagen, Denmark, to be followed by tech transfer to Chiba, Japan, for the next ma...
RA covering establishment and functions of a quality management system and retention of quality system records.
AI is streamlining and accelerating process development and manufacturing, but more work is needed to understand how best to use the technology in compliance with the strict drug p...
Ensuring raw materials are virus-free is still a major challenge for the cell and gene therapy sector. Screening will remain a core quality control strategy as detection and inacti...
Construction of the lab was completed last month and subsequently received approval from the Danish Medicines Agency (DKMA) following an on-site inspection. Laboratory operations w...
Quality control programs in injection molding are often focused on monitoring production – measuring dimensions, tracking variation, and verifying consistency across runs.
These revised reports address two critical aspects of modern drug manufacturing and reflect current regulatory expectations and real world industry experience to help manufacturers...
In 2026, Quality Management Systems (QMS) is no longer merely about regulatory compliance or earning a certification.
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