Shift from approvals to digital intimation via NSWS portal aims to cut timelines and boost innovation in early-stage drug development
The study was conducted by PwC India in line with ISO 14040 and ISO 14044 protocols
PMDA is regarded among the most stringent regulatory bodies globally
The company stated that it will work closely with the regulator to address the observations within the stipulated timeframe
Zero-observation outcomes strengthen global credibility and accelerate CDMO ambitions
Visit underscores push for self-reliance in essential medical consumables and India’s ambition to become a global medtech manufacturing hub
To boost compostable packaging, resin innovation, and supply chain speed
The collaboration will embed OpenAI’s advanced AI systems across Novo Nordisk’s global operations
CDSCO-cleared BSM-5700 series targets ICU, NICU, ER, OR and digital health integration under ABDM
Collaboration aims to align hospital staff learning with NABH 6th Edition standards, patient safety, and measurable quality outcomes
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