CDMO

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Contract Development and Manufacturing (CDMO) Services

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.

From rigorous pharmaceutical synthesis and global collaboration to innovative process development and quality assurance, we strive to deliver excellence and meaningful impact in the world of APIs.

Professional Scientists

Experts in complex chemistry and process development.

Advanced Facilities

cGMP-compliant labs with modern equipment.

Innovative Processes

Optimized methods for cost-effective and sustainable production.

Collaborative Approach

Tailored solutions for global partners.

Partner with Tagoor Labs

Looking for high-quality APIs, advanced intermediates, or custom manufacturing solutions? Contact us to discuss your requirements and explore collaboration opportunities.

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Frequently Asked Questions

Still Have Questions?

What type of products does Tagoor Labs specialize in?

Tagoor Labs specializes in high-quality APIs, advanced intermediates, and key starting materials, with expertise in complex and multi-step chemical synthesis.

How can I collaborate on a custom synthesis project?

You can collaborate by reaching out to our business development team with your project requirements. We evaluate feasibility, share a development plan, and then proceed with transparent deliverables.

Where are your manufacturing facilities located?

Our cGMP-compliant manufacturing facilities are located in Andhra Pradesh, India, with corporate and R&D offices based in Hyderabad.

Do you offer training or internship programs?

Yes, Tagoor Labs provides training and internship opportunities for qualified candidates in R&D, analytical labs, and manufacturing departments, depending on availability.

Which analytical technologies are used?

We use advanced analytical tools such as HPLC, GC, LC-MS, UV, IR, and other modern instrumentation to support method development, validation, and quality testing.

How can I access published research or certificates?

You can request documentation, COAs, DMFs, and research information directly through our support or business enquiry team, who will share the required files securely.

Tagoor Labs is committed to advancing pharmaceutical innovation through high-quality APIs, advanced intermediates, and reliable manufacturing solutions aligned with global standards.

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Our Services

Active Pharmaceutical Ingredients (APIs)
Advanced Intermediates & Key Starting Materials (KSMs)
Contract Development & Manufacturing (CDMO) Services
Research & Development (R&D)
Manufacturing Capabilities