The FDA Law Blog

SEPTEMBER 19, 2023

Industry has long requested input from FDA about the types of patents that can be listed in the Orange Book, and, in response, FDA asked for comments on the types of patents that should be listed. But FDA has never made an affirmative statement as to the types of patents that can be listed in the Orange Book.

FDA 105

FDA Communication Dosage 105

The Checkup by Singlecare

FEBRUARY 1, 2024

Food and Drug Administration (FDA) to treat opioid use disorder and alcohol use disorder. Communicating openly with your healthcare team about all medical conditions you have and medications you take is the best way to identify potential naltrexone interactions. It comes as an oral tablet and intramuscular (IM) injection.

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Communication Dosage FDA 92

pharmaphorum

JANUARY 4, 2022

They also used direct communication, marketing materials, media and financial statements, models and other information to defraud potential investors, according to the complaint. Theranos raised almost $1 billion from investors before the company and its claims were eventually exposed as a sham.

Documentation 52

Documentation Communication FDA 52

European Pharmaceutical Review

SEPTEMBER 22, 2023

Limitations of monoclonal antibody therapies Regulatory approvals from the US Food and Drug Administration (FDA) for aducanumab and lecanemab – and likely very soon for donanemab also – opened a route for different therapeutic modalities and other relevant disease targets, such as tau. Brain Communications.2022;4(1). Wang CY, et al.

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Immunization Vaccines Communication Labelling 97

The FDA Law Blog

JUNE 7, 2023

The “façade of ‘negotiations’ and ‘agreements’” require Merck to communicate that it has “agreed” to an HHS-mandated price, and to endorse the viewpoint that the price is ‘fair’”, when in fact there has been neither a real agreement nor a fair price.

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Communication 45

ISPE

OCTOBER 26, 2022

For example, an assessment for a facility primarily focused on US and EU markets would only consider GMPs and regulations from EudraLex and the FDA. FDA CFR Title 21 Parts 211, 600, and 1271; 8. , FDA Guidance for Industry: Sterile Drug Products Produced by Aseptic Processing–Current Good Manufacturing Practice, 11.

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Vaccines Compounding Documentation FDA 97

The Checkup by Singlecare

DECEMBER 6, 2023

Alcohol and propylene glycol-containing products Similar to concurrent use of alcohol, concurrent use of propylene glycol with metronidazole or within three days after completing metronidazole is considered a contraindication in FDA metronidazole prescribing information.

Dosage 52

Dosage Communication Labelling Hospitals 52