The Regulatory Affairs team at TAGOOR LABS consists of accomplished professionals who have extensive knowledge & in-depth understanding of regulatory regimes of various global regulatory authorities. Besides playing a crucial role in ensuring complete adherence to the country/region specific regulatory requirements, the team has vast experience in the compilation of DMFs, CTD/eCTD Dossiers for submission to regulatory authorities globally including USA/ EU/AUS/JAPAN/BRAZIL/CHINA/CANADA/KOREA/SOUTH AFRICA/MEXICO/NEW ZEALAND, etc.
The regulatory team is continuously updated on the global regulatory framework, essential for organizing data generation as per the submission norms mandated in the respective territories.
TAGOOR LABS supports its customers by providing comprehensive documentation including Drug Master Files for their dosage form applications/ANDA/MAA filings, etc. Our Regulatory Affairs team has extensive regulatory expertise and in-depth understanding of global regulatory framework, thus ensuring adherence and compliance with all the applicable cGMP and ICH guidelines, and regulatory requirements.