Remove Dosage Remove Packaging Remove Webinar
article thumbnail

The key role of GMP analytical testing for drug products

European Pharmaceutical Review

Stability tests are designed to assess the percentage of the active substance throughout the products shelf life and provide insight into any degradation that may occur within the final dosage form. For solid dosage forms, including capsules, tablets, or film-coated tablets, dissolution tests are conducted.

Dosage 64
article thumbnail

Mitigating the risks of cross-contamination during Oral Solid Dose (OSD) manufacturing

Pharmaceutical Technology

Compared to other dosage forms, tablets are simpler to manufacture, package, and transport. Please check your email to download the Webinar. Tablet manufacturing, which is the most common OSD form, takes an API dry powder ingredient and compresses it to form tablets, which can be coated or uncoated.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

The Important Role that Biopharmaceutics Plays in Accelerating Early-Phase Drug Development

Pharmaceutical Technology

Biopharmaceutics is a scientific discipline that examines the interrelationship of the physicochemical properties of the drug, the dosage form in which the drug is given, and the route of administration on the rate and extent of systemic drug absorption ( Applied Biopharmaceutics and Pharmacokinetics, Shargel, Wu-Pong and Yu, 5th Edition ).

article thumbnail

Patient Engagement in Pharma – Why and How?

Viseven

Engagement can lead to improvements in drug delivery methods, packaging designs, and support services that enhance the overall patient experience. This education can be delivered through various formats, such as webinars, videos, and written materials.

article thumbnail

3 of the year’s most notable FDA nods

PharmaVoice

Other PrEP regimens on the market require daily oral dosages or shots every few months, but the latest version is only administered twice a year. The FDA approved the updated formulation, which will be sold under the brand name Yeztugo, earlier this month.

FDA 130
article thumbnail

European Pharmacopoeia Goes Digital

PharmTech

EDQM will host a two-part webinar to present the benefits of the new platform. Information on how to register for the free webinars can be found on EDQM’s website. BASF Opens GMP Manufacturing Facility in Michigan Susan Haigney June 19th 2025 Article The new facility offers cleanroom packaging and high-sensitivity analytical testing.

Dosage 59