ISO Certification highlights commitment to quality for continuous blood glucose monitorRUTHERFORD, N.J., Jan. 21, 2025 (GLOBE NEWSWIRE) -- Glucotrack, Inc. (Nasdaq: GCTK) (“Glucotrack” or the “Company ...

The FDA says that food companies will have until Jan. 15, 2027 to stop using the dye. Drugmakers will have an extra year, until January 2028, to comply with the change. Red 3, also known as ...

To meet FDA expectations and achieve audit success, Indian manufacturers must prioritize compliance with 21 CFR Part 820 now upgraded as QMSR. This involves ensuring data integrity, conducting process ...

The FDA’s Center for Drug Evaluation and Research (CDER) approved 50 new small molecules, biologics and oligonucleotide therapeutics last year. The class of 2024 was a little smaller than that ...

Life sciences manufacturers are bound by regulations such as the FDA’s Current Good Manufacturing Practice (cGMP) and the MHRA’s standards, which necessitate meticulous record-keeping and consistent ...

Manufacturers benefit from consultants' guidance on FDA 21 CFR 820 compliance and the new QMSR standards. Their team assists in setting up and auditing quality management systems (QMS), ensuring ...

Mesoblast (ASX:MSB) was the top performer for the year up 835% (as of December 30). On December 18 Mesoblast announced that the US Food and Drug Administration (FDA) had finally approved its therapy ...

DUBLIN, Dec. 15, 2023 /PRNewswire/ — The “FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers” training has been added to ResearchAndMarkets.com’s ...