Chemcure Facility
Welcome to Chemcure Life Sciences LLP

Excellence in API and Intermediate Manufacturing

A trusted manufacturer of Active Pharmaceutical Ingredient (API) & its Intermediates, supported by strong R & D and Quality capabilities and a state of art manufacturing facility located at Bamanbor GIDC, Rajkot.

We are India’s leading manufacturer of Ambroxol Hydrochloride & Acebrophylline with a combine Production Capacity of 100 MT / Annum.

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Chemcure R&D & Facility
Testimonials

What Our Clients Say

Chemcure Life Sciences is trusted by pharmaceutical companies for reliable API and Intermediate manufacturing, strong R&D support, and consistent quality. Here is what our partners say about us.

Our Process

How We Ensure Quality Manufacturing

Project Assessment

Understanding product requirements and specifications.

R&D Development

Creating safe and scalable processes in our labs.

Manufacturing

GMP-focused production of APIs and Intermediates.

Quality Approval

QC testing and compliant documentation for delivery.

FAQ

Frequently Asked Questions About Our API & Intermediate Manufacturing

  • General & Process
  • Quality & Compliance
  • What products does Chemcure manufacture?
    We manufacture a range of Active Pharmaceutical Ingredients (APIs) and key Intermediates used in various therapeutic categories.
    Do you offer custom synthesis?
    Yes, our R&D and Process Development teams support custom synthesis for new Intermediates and process optimization projects.
    What is your manufacturing capacity?
    Our plant at Bamanbore GIDC is designed for scalable production with dedicated reactor capacities, utility systems, and expansion capability.
    Do you support pilot and scale-up batches?
    Yes, we offer lab-scale development, pilot batches, and commercial scale-up in alignment with customer requirements.
    How do I request technical or commercial information?
    You can contact us through our website or email, and our team will share COAs, specifications, regulatory documents, and quotations.
  • Are your products manufactured under GMP guidelines?
    Yes, our facility follows GMP-focused practices with validated systems, controlled environments, and well-documented procedures.
    What quality checks are performed during production?
    Raw material testing, in-process checks, stability studies, and final QC testing are conducted before batch release.
    Do you provide regulatory support?
    Yes, we provide DMF support, technical packages, validation documents, and audit assistance based on customer requirements.
    How do you ensure batch consistency?
    Controlled processes, SOP-driven operations, validated equipment, and continuous monitoring ensure uniform batch quality.
    Are your products tested for impurities and stability?
    Yes, analytical testing is performed for purity, residual solvents, related substances, and stability to ensure compliance.