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Unlike regulators in India and China, the FDA does not require most generic drug makers to conduct human clinical trials if they can demonstrate that the generic version is chemically equivalent to the original drug
Para finalizar proponen incluso un algoritmo de tratamiento ( figura 2 ) donde todo pacientes con ictus o alto riesgo cardiovascular, debera recibir ar-GLP1, recomendando incluso la suspensin de otras molculas como iDPP-IV por su nulo beneficio pronstico
-Emerging Competitors & Innovators 6
CNNs Tami Luhby contributed to this report.
