Pharmaceutical Technology

NOVEMBER 24, 2022

This is due to the fact that the current Good Manufacturing Practice (cGMP) standards required for human studies involve a significant investment in infrastructure and quality systems in order to efficiently comply with all national and international regulations. What makes Quotient Sciences’ approach to these study types unique?

Bioavailability 130

Bioavailability Manufacturing Drugs Production 130

Pharmaceutical Technology

MARCH 7, 2023

Due to rising healthcare spending, launch of novel treatments, and the rise of chronic diseases in an aging population, the global pharmaceutical packaging equipment market is rapidly expanding. Safety issues must also be addressed, such as containment and potential ignition factors. Recent analysis valued the market [i] at USD 8.5

Production 130

Production Containment Bioavailability Manufacturing 130

Pharmaceutical Technology

FEBRUARY 3, 2023

Additionally, OSD manufacturing approaches are well developed, with processes that ensure a repeatable distribution of ingredients, uniformity in dissolution, and bioavailability, which verify that the drug product is safe and effective. Compared to other dosage forms, tablets are simpler to manufacture, package, and transport.

Contamination 130

Contamination Manufacturing Containment Production 130