State Drugs Controller, Haryana and CDSCO preliminary reports show violations of good manufacturing practices (GMP) by Maiden Pharmaceuticals. A report has been submitted to the Union Health Ministry, which appointed a four-member committee for further investigation. The committee will, after examining and analysing adverse event reports, causal relationships and all related details shared by WHO, suitably advise and recommend DCGI about the further course of action. The committee may co-opt any other technical expert as deemed necessary.
from Top Health News | Latest Health & Healthcare Industry Information and Updates: ET HealthWorld : ETHealthworld.com https://ift.tt/q9eUw6p
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» Centre appoints four-member committee to examine Gambia cough syrup-related deaths
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