This site uses cookies to improve your experience. To help us insure we adhere to various privacy regulations, please select your country/region of residence. If you do not select a country, we will assume you are from the United States. Select your Cookie Settings or view our Privacy Policy and Terms of Use.
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Used for the proper function of the website
Used for monitoring website traffic and interactions
Cookie Settings
Cookies and similar technologies are used on this website for proper function of the website, for tracking performance analytics and for marketing purposes. We and some of our third-party providers may use cookie data for various purposes. Please review the cookie settings below and choose your preference.
Strictly Necessary: Used for the proper function of the website
Performance/Analytics: Used for monitoring website traffic and interactions
This enables us to optimise dosages in our final products, enhancing both bioavailability and patient safety. Some of our clients have successfully implemented strategies such as displaying supplier logos and QR codes on packaging, allowing consumers to easily access information about the ingredients and clinical results.
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.
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.
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 ).
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.
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.
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.
We organize all of the trending information in your field so you don't have to. Join 11,000+ users and stay up to date on the latest articles your peers are reading.
You know about us, now we want to get to know you!
Let's personalize your content
Let's get even more personalized
We recognize your account from another site in our network, please click 'Send Email' below to continue with verifying your account and setting a password.
Let's personalize your content