Inflation and rebates caused wholesale prices on medicines to drop in second quarter (STAT)
Contract research is having a moment right now. Will M&A splashes drive the industry to even greater heights? (Endpoints)
Ziopharm lays off half its staff after manufacturing issues force delays (Endpoints)
Safety fears force Pfizer to change pivotal DMD gene therapy trial protocol (Endpoints)
George Church, his students, and top VCs go nationwide with a biotech training camp (Endpoints)
Looking to rewrite the rules of drug licensing, startup Anji is on the hunt for 'dynamic equity' joint ventures (Endpoints)
Banking on integrase inhibitors as HIV cornerstone, ViiV bags 3rd-generation compound from Shionogi (Endpoints)
On a journey to drastically speed up cell therapy manufacturing, Kytopen lands $30M Series A (Endpoints)
Innovent bets $250M+ on Union's PDE4 inhibitor ahead of a PhII readout (Endpoints)
As supply chain worries ease up, Big Pharma CEOs have a new top concern: recruiting and keeping employees (Endpoints)
MIT cell-engineering spinout nets $30M for mass manufacturing platform (Fierce)
US FDA Guidance On B. Cepacia Contamination Coming Soon, CDER Director Cavazzoni Says (Pink Sheet)
Picture Is Worth 1,000 Meetings: ‘Snapshots’ Could Support ‘Breakthrough’ Dialogue At US FDA (Pink Sheet)
Real-World Evidence Under Consideration For Use In Interchangeable Biosimilars Applications (Pink Sheet)
Medtech
CDRH's 2021 'reset' shunted again as COVID-19 dominates workload (MedtechDive)
Vensana Capital redoubles medtech investment efforts with $325M 2nd fund (Fierce)
Zebra Medical Vision lands FDA clearance for tool to detect cardiovascular disease (Mobihealthnews)
FDA starts review after study finds Boston Scientific's Watchman is riskier in women (MedtechDive)
Borderline And Classification Decisions: New Process Means Six-Month Time Limit – Sometimes (MedtechInsight)
Government, Regulatory & Legal
FTC Deepens Look At $1B Medtronic-Intersect Deal (Law360)
Regulatory Recon is our daily intelligence briefing for the regulatory affairs space, bringing you the top regulatory, biopharma and medtech news stories from around the globe.
A story’s inclusion in Regulatory Recon does not imply endorsement by Regulatory Focus or RAPS.
Adam Fisher, the staff director of the Office of Pharmaceutical Quality in the Center for Drug Evaluation and Research (CDER) at the US Food and Drug Administration (FDA), reported that the agency has approved 17 pharmaceuticals that utilize continuous manufacturing in their production.
The European Medicines Agency (EMA), in partnership with the European Commission (EC) and the Heads of Medicines Agencies (HMA), has published the first quarterly report on the state of clinical trials conducted in the EU and the European Economic Area (EEA). The report is intended to shed light on the progress being made to attract more clinical trials to the region and increase access to new treatments as part of the targets set by the EU in 2025.
An official from the US Food and Drug Administration (FDA) on Monday presented three case studies demonstrating how sponsors effectively utilized real-world evidence (RWE) and real-world data (RWD) to secure approval for their products.