Cefepime Orchid Pharma has been granted by the (DCGI) for its Cefepime and Enmetazobactam antibiotic 2024.
Cefepime Orchid Pharma has been granted approval by the Drug Controller General of India (DCGI) for its Cefepime and Enmetazobactam…
Influence of TMR highlights the significance of being agile and adaptable when addressing regulatory changes.
Influence of TMR highlights the significance of being agile and adaptable when addressing regulatory changes. Influence of TMR highlights the…
The Indian pharmaceutical industry adopts eco-friendly measures to reduce plastic usage and transition to renewable energy sources.
The Indian pharmaceutical industry adopts eco-friendly measures to reduce plastic usage and transition to renewable energy sources. Indian pharmaceutical industry…
Device surveillance he European Unions (MDCG) has released revised guidance on device surveillance-24
Device surveillance the European Unions Medical Device Coordination Group (MDCG) has released revised guidance on device surveillance. Device surveillance The…
Doxycycline:Lupin has received approval from the US FDA to market its Doxycycline for injection-2024
Doxycycline: Lupin has received approval from the US FDA to market its Doxycycline for injection-2024 Doxycycline for injection Global pharmaceutical…
The DCGI underscores the necessity of performing sample tests to verify that medical devices and in-vitro diagnostics (IVDs) comply with established standards-2024
The DCGI underscores the necessity of performing sample tests to verify that medical devices and in-vitro diagnostics (IVDs) comply with…
CDSCO has issued a revised edition of its guidance document pertaining to biologicals.
CDSCO has issued a revised edition of its guidance document pertaining to biologicals. CDSCO has issued a revised edition of…
The US FDA grants priority review to Mercks sBLA 2024 for Keytruda with chemo for metastatic malignant pleural mesothelioma.
The US FDA grants priority review to Mercks sBLA for Keytruda with chemo for metastatic malignant pleural mesothelioma. The US…
EU IDMP Implementation Guide -2_Data elements for the electronic submission of information on medicinal products for human use
EU IDMP Implementation Guide -2 Data elements for the electronic submission of information on medicinal products for human use EU…
Certification of suitability : New requirements for CEP to the Monographs of the European Pharmacopoeia CEP dossier 2.0
Certification of suitability:New requirements for CEP to the Monographs of the European Pharmacopoeia CEP dossier 2.0 New requirements for the…