ADVERTISEMENT

Risk Management

BIOSECURE Act – Which Indian Firms Are Best Placed To Help Plug Pharma’s Sourcing Gaps?

BIOSECURE Act – Which Indian Firms Are Best Placed To Help Plug Pharma’s Sourcing Gaps?

Indian CMOs, CDMOs and CRDMOs are expanding capacity and making leadership moves ahead of the BIOSECURE Act, anticipating demand from big pharma and budding biotechs. Scrip brings details on leading Indian firms which could be potential go-to suppliers for US companies affected by the proposed Act

Latest Philips Recall Linked To Death, Injuries

Latest Philips Recall Linked To Death, Injuries

Philips has issued a recall of various Trilogy ventilators due to safety issues that may affect their ability to properly function. The US FDA has designated the recall class I, its most serious.

CAR-T Therapies: Stakeholders Urge Rethinking Of Postmarketing Requirements And REMS

CAR-T Therapies: Stakeholders Urge Rethinking Of Postmarketing Requirements And REMS

Long-term follow-up requirements have taken a conservative approach, but could be ripe for re-examination and global harmonization, Kite Pharma executive director says, while former FDA gene/cell therapy office head Wilson Bryan wants the classwide REMS eliminated.

EMA Explains How To Make Risk Minimization Measures Robust & Effective

EMA Explains How To Make Risk Minimization Measures Robust & Effective

Pharmacovigilance experts speaking at an event organized by the European Medicines Agency discussed the rationale behind revised requirements relating to how drug sponsors must develop and evaluate risk minimization measures and thereby improve the safety of their medicines.

Mammograms Should Inform Women About Breast Density, FDA Says

Mammograms Should Inform Women About Breast Density, FDA Says

The US FDA now requires mammograms include information about breast density, a significant factor that raises breast cancer risk and can hide tumors.

Veozah Warning On Liver Injury Could Present New Commercial Roadblock

Veozah Warning On Liver Injury Could Present New Commercial Roadblock

The US FDA updated labeling for Astellas’ drug for hot flashes after a postmarketing report of a single patient with signs and symptoms of liver injury taking the medicine. 

‘Inside Regulatory Affairs’ With Bayer Consumer Health’s Jenny Holmes

‘Inside Regulatory Affairs’ With Bayer Consumer Health’s Jenny Holmes

In this installment of HBW Insight’s “Inside Regulatory Affairs” series, Bayer Consumer Health’s global regulatory director, Jenny Holmes, describes how the job has changed in recent years to assume an enabling role for innovation.

Psychedelic Truffles Sold As Supplements Under Scrutiny In Europe

Psychedelic Truffles Sold As Supplements Under Scrutiny In Europe

The increasing prevalence of psychedelic truffles sold as food supplements purported to enhance mood and boost creativity is of growing concern to the European Food Safety Authority. EFSA’s Milen Georgiev tells HBW Insight how the authority is handling this emerging risk to consumers.

Six Deaths Linked To Inari Clot Removal Device

Six Deaths Linked To Inari Clot Removal Device

Inari Medical is updating use instructions for a clot-removing catheter due to the potential for serious adverse effects, including death.

Arrested Astellas Employee Indicted In China

Arrested Astellas Employee Indicted In China

An employee of Astellas in China first detained 17 months ago on suspicion of espionage has been formally indicted and now faces trial.