Pharmaceutical Technology
AUGUST 22, 2022
They also offer enhanced bioavailability, exact dosing and an extended shelf life. Fixed-dose combination (FDC) systems aim to increase patient compliance in therapies involving two or more active drugs. Softgel capsules, containing a liquid, paste or emulsion active ingredient, are trusted and favoured by many patients.
XTalks
JANUARY 30, 2025
Benefits of Oral Liquid Dosage Forms Paediatric dosage forms (PDFs) provide considerable advantages over traditional oral solid dose (OSD) products, particularly in terms of improving patient compliance and ensuring therapeutic effectiveness. One of the most significant benefits of PDFs is their ease of administration.
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XTalks
FEBRUARY 5, 2025
Attendees will learn how to enhance differentiation, ensure regulatory compliance and drive success in this rapidly evolving field. The HALO platform enhances peptide half-life, facilitating monthly dosing and titration-free regimens, while the MOMENTUM platform optimizes oral bioavailability. billion in 2024 to $37.94
Camargo
DECEMBER 22, 2021
Clinical pharmacology may also involve comparative bioavailability analyses, which are generally required for drug formulation bridging studies, to demonstrate bioequivalence. These are put in place to ensure product quality in compliance with FDA requirements. Biowaiver Eligibility.
Pharmaceutical Technology
JUNE 14, 2023
Many small and mid-cap companies lack the expertise for regulatory compliance and high containment facilities and thus seek to outsource NMEs (New Molecular Entities) requiring special handling. A number of high-impact milling methods, including ball, hammer, pin, and disc mills, have been adopted to meet this need.
Cloudbyz
MARCH 5, 2024
Administration and Dosage: Due to their nature, biologics are often administered via injection or infusion, which can affect patient compliance and convenience. Oral Bioavailability: Developing small molecules that are effectively absorbed when administered orally, while also being stable in the digestive system, can be complex.
Camargo
SEPTEMBER 30, 2021
Drug product formulation should be as simple as possible, but carefully executed to account for the characteristics of the intended administration route and dosing regimen and to facilitate successful manufacturing, storage, shipping, and compliance in the clinic and eventually on the market. Species Selection. Case report format and design.
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