The inspection concluded with zero observations, confirming the facility's compliance with current Good Manufacturing Practices
The EIR was issued following an inspection of the facility from November 10 to November 21, 2025
This transaction fundamentally strengthens Scinai's CDMO platform
The program provides pharmaceutical manufacturers with auditable, primary emissions data and verified proof of a 30% CO? reduction across DFE Pharma’s lactose portfolio
A PhD in Pharmaceutical Sciences, Dr Singh has led global regulatory audits, product validations, and quality systems spanning therapeutic formulations, dietary supplements, and functional foods
Experts caution that realizing AI’s potential requires careful management and risk mitigation
India should explore Sustainability-Linked Incentives (SLI) targeting innovations in the 12 principles of green chemistry
India’s traditional medicine systems have also earned formal recognition in key bilateral trade agreements
The company views ESG reporting as a strategic tool to build trust with clients, investors, regulators, and stakeholders worldwide
Nona aims to help global biopharmaceutical companies fast-track clinical trial initiation without compromising scientific rigor or quality standards
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