International – EMA-FDA parallel scientific advice program has ‘limited’ uptake

A review of the last five years of the Parallel Scientific Advice (PSA) program between the US Food and Drug Administration (FDA) and the...
Topical Drug Products for Cutaneous Application: Human Safety Assessment Guidance

USA – FDA warns pharmacy benefit company for distributing unapproved foreign drugs

The US Food and Drug Administration (FDA) recently warned pharmacy benefit firm ElectRx for substituting prescription drugs ordered by its customers with drugs sourced...

International – Bébé-Crispr : la modification du génome d’embryon bute sur des obstacles techniques

Une décennie après son déferlement dans les laboratoires, l’outil de modification du génome Crispr-Cas9 alimente toujours une révolution scientifique et médicale et continue de...
MHRA Offers Grace Period for Device Manufacturers Dealing With Withdrawn Notified Bodies

UK – Pholcodine-containing cough and cold medicines: withdrawal from UK market as a precautionary...

Pholcodine-containing cough and cold medicines are being withdrawn from the UK market as a precaution following a review which found that their benefits...

USA – FDA approves first treatment for Rett Syndrome

FDA has approved Daybue (trofinetide) oral solution as the first treatment for Rett syndrome, a rare, genetic neurological disorder. Daybue is approved for the...

USA – Pfizer: le spray nasal anti-migraine approuvé par la FDA

Pfizer a annoncé vendredi que la Food and Drug Administration (FDA) américaine avait approuvé le Zavzpret, son spray nasal pour le traitement de la...

Europe – EMA Q&A addresses submission of data elements for raw data pilot

The European Medicines Agency (EMA) this week issued a question-and-answer guidance to address sponsors’ questions on its pilot testing the review of raw clinical...

USA – Generic drugmakers seek clarity on pre-submission facility correspondence

Drugmakers want clarifications on an updated draft guidance the US Food and Drug Administration (FDA) recently released on pre-submission facility correspondence (PFC) for generic...

Europe – Regulatory, industry panels address EU GMP Annex 1 implementation

Pharmaceutical manufacturers in the EU may have to approach the manufacturing of sterile drugs a little differently under the EU’s Annex 1 covering good...

UK – Novo Nordisk’s weight-loss drug recommended by NICE

Patients will inject themselves once a week with pens pre-filled with semaglutide, also know as Wegovy. The drug will be offered alongside a reduced...