The Pharmaceuticals and Medical Devices Agency (PMDA) is reviewing the risk of anaphylaxis for G-CSF preparations including Gran (filgrastim) and its biosimilar versions - a move that is likely to result in label changes. Other G-CSF preparations under review are…
To read the full story
Related Article
- G-CSF Preparations Ordered to Add Anaphylaxis in ADR List
September 14, 2016
REGULATORY
- Pharma Urges Pricing Rewards to Bolster Japan’s Drug Discovery Strength
September 24, 2026
- New Digital Minister Furukawa Pledges Push for Healthy Longevity
September 24, 2026
- MHLW Eyes Higher Long-Term Care Premiums for Wealthier Seniors
September 24, 2026
- Nippon Ishin’s Urano Named Senior Vice Health Minister in Takaichi Cabinet
September 24, 2026
- Ueno Vows to Advance Drug Innovation, Advanced Medicine in 2nd Term
September 24, 2026
We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…





