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Pharmaceutical APIs and Intermediates.

Narmada Organics

The Hub Of APIs

Narmada Organics is new entrepreneur in Active Pharmaceutical Ingredients (APIs) and Pharmaceutical Intermediates having GMP and AHU Facilities in Manufacturing Unit, established in 2020, Located at Plot No. C-345/2 GIDC of Saykha (The Emerging Chemical Hub of India) of Gujarat

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API Manufacturing

Active Pharmaceutical Ingredient (API) is the biologically active component of a drug product (tablet, capsule, cream, injectable) that produces the intended effects.

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Impurity Synthesis

Impurity profile studies play significant roles in active pharmaceutical ingredient (API) development, which are closely related to the quality, safety and efficacy of drug products.

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Contract Manufacturing

Contract manufacturing involves production of goods by firm, under the label of another firm.Contract manufacturers provide such service to several firms based on their own or consumers specifications.

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About Us

We at

Narmada Organics

Make New Discoveries We provide you with a solution.

Narmada Organics is committed to the highest quality standard, safety and protection of its members and the environment. Our APIs are specified and analyzed according to relevant pharmacopoeias and Enterprise standards.

  • Benchmark quality
  • Partnership and collaboration
  • Cost effective process development
  • Highly Enthusiastic & Experienced Team
  • Continuous learning & knowledge sharing
  • Environmental safety & social responsibilities.
  • Environmental Testing
  • Focus on innovation by modernization
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API Manufacturing

Active Pharmaceutical Ingredient (API) is the biologically active component of a drug product (tablet, capsule, cream, injectable) that produces the intended effects.

Impurity Synthesis

Impurity profile studies play significant roles in active pharmaceutical ingredient (API) development, which are closely related to the quality, safety and efficacy of drug products.

Custom synthesis and process development

Contract manufacturing involves production of goods by firm, under the label of another firm.Contract manufacturers provide such service to several firms based on their own or consumers specifications.

Scale up studies for any given process

The goal of scale-up is to identify & develop a process that will successfully produce a desired product when manufactured at a commercial scale.

Process Optimization.

the process by which manufacturers look for ways to improve their manufacturing process. A product's or system's optimization can take place on several levels.

Scale-up production from a few kgs to tons

Scaling up production to deliver more quantity of the product. Delivering with the same quality and efficiency.

Regulatory documentation, including DMFs (CTD format)

We Regulatory give documentation of our products with Drug master file. DMF the set of series of information for an Active Pharmaceutical Ingredient (API) or Drug substance brought together in CTD format as per regulatory requirements.

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Performance

Manufacturing Facilities

SSR Reactors

SSR Reactors Capacities from 0.5KL to 5KL

GLR Reactors

Capacities from 0.5KL to 5KL

Gas Absorbers

Gas Absorbers High Efficiency Scrubbing system

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We'll ensure you always get the best Results

+91 94091 33000 (Pratik Devani)

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