XTalks

JUNE 1, 2022

BONESUPPORT has recently received market authorization from the US Food and Drug Administration (FDA) for Cerament G, its bone graft with antibiotic elution. Xtalks learned more about BONESUPPORT and its first FDA-approved drug-device combination product Cerament G through an email interview with BONESUPPORT’s CEO Emil Billbäck.

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Filler FDA Approval Production Marketing 98

The Pharma Data

NOVEMBER 30, 2020

30, 2020 – Nearly 15% of talc-based cosmetic products analyzed in a recent study contained asbestos. She noted that EWG’s online database has identified more than 2,000 personal care products that contain talc, including more than 1,000 loose or pressed powders that could pose an inhalation risk. MONDAY, Nov. © 2020 HealthDay.

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Containment Production Cosmetics Contamination 52

Pharmacy Checkers

NOVEMBER 12, 2020

The new federal rule on drug importation from Canada , drafted pursuant to Section 804 of the FDCA, does not allow for the importation of foreign versions of FDA-approved drugs. It only allows for the importation of FDA-approved drugs. Prescription Drug Importation.” Bollyky and Aaron S. to $750 a pill overnight.

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FDA Approval Drugs Filler Manufacturing 62

Pharmaceutical Technology

MAY 10, 2023

Most molecules absorb light in the IR region of the electromagnetic spectrum, converting it to molecular vibration, and this absorption characterises the nature of the chemical bonds contained in a sample. Bruker Optics’ HYPERION II removes this limitation and enables both IR laser imaging and μ-FT-IR to be carried out using one system.

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Contamination Filler Bioavailability Production 130

The Pharma Data

OCTOBER 22, 2021

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. About Novartis Novartis is reimagining drug to ameliorate and extend people’s lives.

Vaccine 52

Vaccine Vaccination Filler Manufacturing 52

The Pharma Data

DECEMBER 27, 2020

million people misused prescription opioids in 2018, and many die every day from opioid-related drug overdoses. Current intraarticular anti-inflammatory treatments for OA have potentially toxic side effects and may lead to the destruction of cartilage filler proteins. According to the US Department of Health and Human Services, 10.3

Trials 40

Trials Clinical Trials Clinical Trials Containment 40

The Pharma Data

NOVEMBER 4, 2020

. Juyou will be responsible for the overall clinical development and regulatory filings for Pliaglis with the National Medical Products Administration (the “NMPA”, formerly the China State Food and Drug Administration). million and US$1.8 million. . Juyou Bio-Technology Co.,

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Licensing Licensing Dermatology Production 40