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Manufacturing

Manufacturing Facility

Vanquest Pharma API facility is located at Boisar, 100 kms away from the financial capital of India - Mumbai. This plant, spread over 10,500 Sq.mt. Vanquest Pharma has established world class infrastructure for manufacturing APIs complying with the requirements of regulated and semi-regulated markets.

Below is Phase 1 And Unit 1 Equipment List:-
  • Five Stainless Steel cGMP Reactors of 6.3KL , 5KL , 3KL And 2KL Capacities.
  • Eleven Glass Lined Reactors of 6.3KL , 5KL , 3KL , 2KL , 1KL And 0.25KL Capacities.
  • We Have Four cGMP Rotocone Vacuum Dryer , Three cGMP Fluidized Bed Dryer And Twelve Trays of cGMP Vacuum Tray Dryer.
  • We Also Have Six cGMP Centrifuges Filteration , Four cGMP Neutche Filter And Sparkler Filters cGMP.
  • Multi Mill , Shifter cGMP.
  • ETP Capacity 100 CMD (cubic meter per day ).
Our Infrastructure
  • Modern QA, QC, Microbiological and PD Lab supported with high-tech equipment.
  • Capabilities for gram level to kilo level.
  • Fully automated electronically controlled operating system as per GAMP (Good Automated Manufacturing Practice).
  • Effluent Treatment Plant (ETP) with a capacity of 100 CMD (cubic meter per day)..
  • Total reaction capacities - 451MT Per Year.
Technical Expertise
  • A team of 60 scientists (both in Synthesis and Analytical) working round the clock at our API - R&D center.
  • Other support staff include Regulatory and Project Management.
  • Our Analytical team comprises scientists and lab assistants with experience of handling all the latest analytical equipment. We also have a specialized team with vast experience in method development and validations, which supports the robustness of product specifications and compliances as per the requirement.
  • Vanquest Pharma ensures adherence and compliance with all the applicable cGMP and ICH guidelines and regulatory requirements.
  • Our Regulatory team act as a liaison with regulatory agencies and provide expertise & regulatory intelligence in translating their requirements into practical workable plans. They also evaluate products and their ROS in line with regulatory guidelines and prepare valid DMF for submissions.
Quality Policy
  • Vanquest Pharma is committed in manufacturing and supplying the APIs to meet the established requirements of customers and applicable statutory and regulatory requirements.
  • We will strive to enhance satisfaction of our customers by effective application of process approach to improve each of our processes.
  • We will effectively involve all our employees and vendors in our effort to exceed customer expectations.
  • Various training methodologies are used for imparting learning such as instructor led training, experiential learning, simulation based learning, activity oriented learning, e-learning , case study based approach etc.
  • Our induction and handholding itself starts with a structured onboarding to acclimatize the new employees to our products/ processes/ culture and ensure a smooth transition into the organization.
  • Other than formal and structured training interventions, our leaders and managers continuously provide informal mentoring to their team members to groom them for growth and larger roles.
Research & Development
  • The API Research & Development division is an integral component of Vanquest Pharma.
  • The main emphasis is on development of non-infringing process and achieving cost efficiency through process optimization with ability to perform complex reactions.
  • R & D/TTD Team have the capability to deliver quality products within established timelines.


Through Vanquest Pharma we seek to leverage our wide experience in International Marketing, our proficiency in scientific documentation and our ability to speedily secure regulatory approvals to make significant inroads in mark across the world.



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CORPORATE ADDRESS:-

FACTORY ADDRESS:-

PLOT NO. F-10/1, M.I.D.C. TARAPUR, TAL & DIST:- PALGHAR - 401 506.