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BENEO’s galenIQ™ 721 filler-binder optimizes the production of fizzy tablets and powders

Pharma Mirror

This filler-binder enablespharmaceutical and nutraceutical manufacturers to target consumers that have difficultyswallowing standard tablets. As a non-hygroscopic, water-soluble and directly compressibleexcipient, galenIQ™ 721 also provides high content uniformity and production efficiency foreffervescent applications.

Filler 100
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Medical Aesthetics: “Redefining Beauty through Medical Expertise”

Roots Analysis

Medical aesthetics is a growing area of modern medicine that focuses on improving the cosmetic appearance of an individual through various medical treatments. Afterwards, in 2003, the FDA approved Hyaluronic Acid Fillers (HA dermal fillers), bringing the much-anticipated innovation to all types of face and non-face augmentation products.

Filler 40
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EU probes low platelet safety issue with COVID-19 shots

pharmaphorum

Several cases of immune thrombocytopenia – a disorder characterised by low levels of blood platelets that can lead to bruising and bleeding – were reported in the European Medicines Agency’s safety surveillance database.

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Aesthetic Alchemy: “Artistry of Medical Aesthetic Procedures”

Roots Analysis

Medical Aesthetics is an area of modern medicine that specializes in improving the outer appearance of an individual without surgery. It is interesting to note that medical aesthetics companies are continuously enhancing their product portfolio to provide solutions based on the needs of the end user.

Filler 40
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Novartis signs new initial agreement with BioNTech to support fill and finish of the mRNA Pfizer-BioNTech COVID-19 vaccine

The Pharma Data

Novartis blazoned moment that it has inked an original agreement to work its manufacturing capacity and capabilities to address the COVID-19 epidemic by expanding its support of the filler and finish of the Pfizer-BioNTech COVID-19 vaccine. This new agreement follows a first contract inked before this time.

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PRAC investigates heart inflammation reports with Pfizer vaccine

The Pharma Data

During an early May meeting, the European Medicines Agency’s safety committee concluded two reviews of safety signals related to COVID-19 vaccines, while it continued following other vaccine-related “topics of interest.” Separately, EMA’s human medicines committee has begun a rolling review of another monoclonal antibody to treat COVID-19.

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New Section 804 Drug Import Rule Does Not Allow Foreign Versions of FDA-Approved Drugs

Pharmacy Checkers

Kesselheim and Bollyky write: “FDA approvals are specific to the information in the NDA or ANDA, including: the manufacturer, product, and its use; manufacturing location, formulation, source, and specifications of active ingredients; processing methods; manufacturing controls; labeling; and appearance.”. It’s a great plan!