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Unicor Pharmatech LLP
Pioneering Quality and Innovation

Established in 2023, Unicor Pharmatech LLP is a fast-growing pharmaceutical manufacturer operating a state-of-the-art facility built in compliance with global standards, ICH guidelines, and GMP requirements.

Spanning 9,814 square meters, our modern pharmaceutical manufacturing facility is strategically situated on the Gandhidham–Mundra National Highway in Kutch, Gujarat, India, offering excellent logistical advantages with direct access to three major ports — Mundra, Kandla, and Tuna. This prime location ensures smooth, reliable, and cost-effective global distribution to our international partners.

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Director
Mr. Rushi Akhani

Mr. Rushi Akhani is a visionary Director with 13+ years of extensive industry experience, known for his strong leadership, strategic planning, and results-driven approach. Over the years, he has played a key role in driving organizational growth, streamlining operations, and building high-performing teams. His deep expertise, forward-thinking mindset, and commitment to excellence continue to guide the company toward sustained success and innovation.

As the Director of Unicor Pharmatech LLP, he is instrumental in shaping the company’s long-term vision and strengthening its presence in the pharmaceutical and healthcare sector. He focuses on quality-driven processes, regulatory compliance, and sustainable business practices. Under his guidance, Unicor Pharmatech LLP continues to expand its capabilities, foster innovation, and deliver reliable solutions that meet global industry standards.

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Our Milestone
A journey marked by innovation, compliance, and consistent growth in the pharmaceutical and healthcare technology sector.
2014
Initiation of domestic marketing operations
2019
Planning and conceptualization of the manufacturing facility.
2020 - 2021
Commencement and execution of construction of the manufacturing facilities.
2023
Manufacturing facility approval issued by the State FDA.
January 2024
  • WHO-GMP certification issued.
  • Regulatory approval issued by the Democratic Republic of the Congo.
  • Approval issued by the Ministry of Health, Cambodia.
  • 2025
  • Manufacturing facility approval issued by the Pharmacy and Poisons Board (PPB), Kenya.
  • Approval issued by the National Drug Authority (NDA), Uganda.
  • Regulatory approval issued by the Ministry of Health, Liberia.
  • Delivering quality at scale, across every dosage form Measuring Success Through Key Metrics
    38+
    Countries
    472.5Million
    Capsules per year
    1575Million
    Tablets per year
    36.75Million
    Liquid orals
    31.5Million
    External Preparation
    15.75Million
    Units of sachets and dry powder per year
    Why Choose Unicor Pharmatech
    Because quality, compliance, and commitment define everything we deliver to our partners and customers.
    • Comprehensive Dosage Form Expertise
    • World-Class Manufacturing Infrastructure
    • Stringent Quality & Regulatory Compliance
    • Scalable Production Capabilities
    • Expertise in Diverse Therapeutic Segments
    • Reliable Partner for Global Markets
    12+
    • 12+
    • Years Of Experience
    Frequently Asked Questions
    Find clear answers to common questions about our products, processes, quality standards, and business partnerships.
    • What dosage forms does Unicor Pharmatech manufacture?
      We manufacture capsules, tablets, powder sachets, oral liquid formulations, and topical products.
    • Does Unicor Pharmatech offer contract manufacturing services?
      Yes, we provide end-to-end contract manufacturing solutions for domestic and international clients.
    • Are your manufacturing facilities GMP compliant?
      Yes, our facilities strictly follow Good Manufacturing Practices (GMP) and quality regulations.
    • Can you handle large-scale production requirements?
      Absolutely. Our infrastructure supports high-volume production while maintaining consistent quality.
    • Do you manufacture customized formulations?
      Yes, we offer customized formulation development and manufacturing based on client requirements.
    • What quality control measures are followed?
      We follow stringent in-process and finished-product quality testing to ensure compliance and safety.
    Our Accreditations
    Certified, compliant, and trusted—our operations align with recognized national and internationalquality standards.
    FDA
    FDA
    MOH - CAMBODIA
    MOH - CAMBODIA
    ACOREP D R CONGO
    ACOREP D R CONGO
    NDA UGANDA
    NDA UGANDA
    LMHRA LIBERIA
    LMHRA LIBERIA
    WHO - GMP
    WHO - GMP
    ISO 9001:2015
    ISO 9001:2015
    PPB KENYA
    PPB KENYA
    Under Pipeline
    FDA GHANA
    FDA GHANA
    FDA PHILIPPINES
    FDA PHILIPPINES
    TMDA TANZANIA
    TMDA TANZANIA
    KIMADIA IRAQ
    KIMADIA IRAQ
    ZAMRA ZAMBIA
    ZAMRA ZAMBIA
    EFDA ETHIOPIA
    EFDA ETHIOPIA
    KURDISTAN IRAQ
    KURDISTAN IRAQ
    MOH VIETNAM
    MOH VIETNAM
    NAFDAC NIGERIA
    NAFDAC NIGERIA
    Your Trusted Pharmaceutical Manufacturing Partner
    Delivering reliable pharmaceutical solutions through quality, scale, and innovation
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