REGULATORY
PMDA Reviewing Osteoporosis Treatment Forteo for Risk of Shock, Anaphylaxis
The Pharmaceuticals and Medical Devices Agency (PMDA) announced on June 13 that it is reviewing the risk of shock and anaphylaxis associated with Eli Lilly Japan’s osteoporosis treatment Forteo SC Injection Kit 600 μg (recombinant teriparatide). Certain safety measures including…
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REGULATORY
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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…





