Our Services


Taj Active Ingredient Services

TAJ API process chemistry team is capable of solving the most complex chemical development issues in a fast and efficient manner. A distinguishing feature of our team is the equal balance between experienced process and analytical chemists. We are focused on developing safe, scalable processes and have an excellent track record of providing innovative solutions to drug development companies across the globe. We offer fully-integrated contract research, discovery and development services including Drug Discovery, ADMET-PK, Bioanalysis and Process Chemistry & GMP API manufacturing.

Taj API – Taj Pharma Group

One of the largest Active Pharmaceutical Ingredients (API or Bulk Actives) manufacturer in Asia, Taj Pharmaceuticals Ltd;
has commercialized over 200 APIs*. Mammoth capabilities and uncompromising product quality underline the core
competence of the Company.

Total Quality Management is the very essence of Taj Pharmaceuticals Ltd; Every detail is subjected to scrutiny –
be it cGMP compliance, validation, stability studies, documentation, safety, health or environmental issues.
This steadfast adherence to TQM has been highly rewarding and ensures that all products are truly world class.

Taj Pharmaceuticals Ltd; derives its volume in API from the following segments.

Taj Pharmaceuticals Ltd. bulk drug complex located at Vapi (State of Gujrat) is one of the largest integrated antibiotic manufacturing complexes in its class. This facility specializes in the manufacture of cephalosporin API’s (Active Pharmaceutical Ingredients) and has an installed manufacturing capacity of over 800 MT per annum. Set in a total land area of nearly 50,000 sq. mts., this facility is a massive, state-of-the-art, most modern manufacturing complex that produces a wide range of new generation cephalosporin bulk actives.

This facility has over 85 reactors of varied metallurgy including titanium, cast alloy, graphite, PVDF and PTFE with over 300 kl of handling capacity together with several centrifuges, driers and varied production equipment. The facilities are versatile and are capable of carrying out varied reactions ranging from -70°c to +150°c.

Taj Pharmaceuticals Ltd. is known for its world-class crystallisation and lyophillisation facilities, which provide a global competitive edge in sterile product manufacture. Taj also has a unique spray drying facility, which ensures the lowest levels of moisture content.

Taj Pharmaceuticals Ltd. has the capability to handle highly complex and hazardous reactions with utmost safety and productivity. Taj operations are backed by a full spectrum of utilities including a captive power generation plant, high technology solvent recovery facilities, sophisticated quality control equipment and a ‘zero discharge’ environment-friendly effluent treatment plant.

Business today face far more competition and external influences then they did five to 10 years ago. Competing in today’s global economy can be tough for the small to midsize business (SMB). Smaller organization faces the same market pressure as the Global 2000. They are challenged by the need the customer and compliance mandates, manage supplier effectively, control Costs, and gain new customers to grow the business.

For the majority of firms in this industry, the actual manufacture of drugs is the last stage in a lengthy process that begins with scientific research to discover new products and to improve or modify existing ones. The R&D departments in pharmaceutical and medicine manufacturing firms start this process by seeking and rapidly testing libraries of thousands to millions of new chemical compounds with the potential to prevent, combat, or alleviate symptoms of diseases or other health problems. Scientists use sophisticated techniques, including computer simulation, combinatorial chemistry, and high-through-put screening, to hasten and simplify the discovery of potentially useful new compounds.

Why choose us

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