Pharma Manufacturing Companies India

We have an advanced infrastructure, which helps us in offering a flawless range of small volume parenterals in ampoule & dry powder vial form to our esteemed clients. Our unit’s functioning zones are manned by a team of experts and the entire infrastructure is segregated into different departments for streamlining pharma manufacturing, research & Development, packaging, storing, marketing and other related processes. Further, these departments are equipped with the latest equipment & technology that assist us in delivering a quality range of products to the customers

 

Facility Highlights

  • Our critical pharma manufacturing and filling is carried out under Grade A (class 100) with surrounding area of Grade B (class 1000).
  • Our Component preparation , Ampoule & Vial washing area is CLASS C { class 10000}
  • Production & Micro lab area is created with clean room G.I powdered coated sheets with walk-able false ceiling.
  • Air Handling Units (AHU’s) and action ac heating service, Dehumidification Unit and Temperature Control ling as per WHO GMP norms.
  • Movement of the material is made through Mobile Laminars & Dynamic Pass boxes only
  • Automatic & Plc based machines are installed
  • Segregation of every critical processing activity in each zone, to avoid cross-contamination. Respective zones, areas and even uniforms marked with specific colors to ensure total segregation.
  • Total production area and microbiology lab is having Epoxy flooring.
  • The installed production capacity is 1,00,000 ampoules & 50,000 dry powder vials in an 8 hour shift
  • All utilities are provided through walk-able service area.
  • Our in-house quality control department is independent, self-sufficient and capable of carrying out all tests.
  • The facility is dedicated for General small volume parenterals & dry powder injectables.
  • High power generators are available for full time back up of electricity to ensure the plant to run 24hrs operations uninterruptedly.
  • Quality System and Master Validation Plan is strictly adhered