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Our contract development capabilities comprise of co-development of processes, process optimisations, technology transfer and development of pipeline products. We are also engaged in a range of value-adding research activities, both in-house as well as in collaboration with our partners.
We are committed to manufacture products in total compliance with cGMP (Current Good Manufacturing Practices) requirements and match customer expectations. All processes and manufacturing operations are in accordance with the regulatory framework established by ICH (Q7). Our three manufacturing facilities are well-equipped with advanced systems and follow stringent quality and regulatory protocols to ensure that the APIs and Advanced Intermediates manufactured here are only of the highest quality and purity.
Our considerably large manufacturing infrastructure helps us to meet the diverse volume requirements efficiently and effectively. TAGOOR LABS has the capability and the flexibility to manage projects that range from ‘Grams to Tons’ with rigorous system checks and project control to ensure strict confidentially.
Currently, we are a go-to partner for high-quality APIs and Advanced Intermediates and KSMs, for several top pharmaceutical companies in the realm of CDMO services.
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