European Pharmaceutical Review

JULY 5, 2023

The long-awaited PDA TR 43 report provides an approach to a quality decision-making process and represents best practices for the identification and classification of visual nonconformities for (empty) glass containers as pharmaceutical product packaging.

Pharmaceutical Manufacturing

FDA Law Blog: Biosimilars

JULY 15, 2025

This definition is familiar to drug manufacturers because it is substantially identical to the definition that has existed under the MDRP since 2007. The manufacturer’s documentation of the methodology used to determine fair market value would have to be submitted, along with other reasonable assumptions, to CMS each quarter.

Documentation

The Thyroid Pharmacist

JULY 29, 2022

Feel free to use my own health timeline as a guideline to document your health journey. Most filter manufacturers have pictures on their filter packaging that indicate what they will and will not filter, along with the MERV rating. 2007-00313. 2007; 41(6) 1230-1236. Invest in a High-Quality Portable Air Filter.

Health and Personal Care Stores

Pharmacy Friday Pearls

AUGUST 29, 2022

2007 Prospective observational review (n=7) 50 mL of 50% IV dextrose was followed by a loading dose (1 unit/kg) of IV short-acting insulin and a insulin maintenance infusion (0.52.0 mmol/L) There was no documented blood glucose concentration <100 mg/dL recording during the first 12 hrs of HIET. Greene et al., High-dose insulin.,

Packaging