• Unit I-Pharma Impex Laboratories Pvt.Ltd.(Behala Plant):
    • M/s Pharma Impex Laboratories Pvt. Ltd., a pharmaceutical manufacturing unit, situated at Behala Industrial Estate, 620 Diamond Harbour Road, Kolkata – 700 034, initiated in the year 1977 as a private limited company under the Companies Act, 1956 on the objective of production of pharmaceutical formulations in the various dosage forms: Capsules and Small Volume Parenterals (SVP) in the form of Sterile Powder For Injection.

      It is a fast growing pharmaceutical unit, which is well equipped with modern equipments and instruments in line with the standard of WHO-GMP. The organization is engaged in the business of manufacture and supply of the pharmaceutical formulations under the license granted by the Directorate of Drugs Control, Govt. of West Bengal and Drugs Control General of India following Schedule M as per Drugs & Cosmetics Act, 1940 and Rules 1945 there under and all other statutory regulations.

      The company is manufacturing drugs for sale as specified under Schedule C and C1 viz.

      Small Volume Parenterals ( β Lactam Dry Powder-Penicillin group) section
      Capsules ( β Lactam) section

  • Unit II-Pharma Impex Laboratories Pvt.Ltd.(Baruipur Plant)
    • Pharma Impex Laboratories Pvt. Ltd. Baruipur,

      is a leading fast growing professionally managed Pharmaceutical Company with operating Head Office in Park Street Kolkata, India. It has Two Manufacturing Plants. We are pleased to introduce ours that, we set up a manufacturing unit to produce I.V.FLUIDS, situated at South Uttarbhag, Ramnagar Baruipur, Dist. 24 PGS (S)-, West Bengal, is Very Near to Kolkata. Under the name Pharma Impex Laboratories Private Limited (II Unit). The plant has been designed as per W.H.O. G.M.P. norms have certified by GMP, GLP, WHO and focus on International regulatory approvals.

      The Pharma Impex Laboratories Private Limited for the manufacture of Life saving Drugs (IV Fluids) of international quality in L.D.P.E bottles using Form- Fill- Seal (FFS) technology. For the manufacturing of the I.V. Fluid bottles, the containers are formed, filled and sealed mechanically in a close sterile chamber. The Entire manufacturing facility is designed and constructed as per the Drugs and Cosmetic Act 1940 and Rules there under. The entire process is free from any type of pathogenic organisms, human contact and atmospheric exposure. The High-tech filtration system and super sophisticated terminal sterilization system renders the solution sterile and pyrogen free. The Manufacturing facilities of Company environment as per WHO GMP and revised Schedule M.

      The container is preparing by using Pharmaceutical grade pure virgin LDPE granules. The Water for injection which we use having high quality through new innovative techniques like Softening, Multi grade filtration, Reverse Osmosis process, Electronic De-Mineralization and Multi Column Still. Distillation & Condensation at a temp. of 165ºC and maintaining WFI temp as above 80ºC, is circulated continuously through loop line and is free from all type of contaminations like bacteria fungus and Pyrogen. We are maintaining the quality of product by using high quality approved raw materials and filtration through 5µ, 0.45 µ and 0.22µ filters. The major process in I.V. Fluid manufacturing is Sterilization, for that we using super sophisticated Equipment which called as Super Heated Water Spray Sterilizer at validated time and temperature.

      We have sophisticated in-house Laboratory for the analysis of Raw materials, Packing materials, Process materials and Finish goods. Physical, Chemical & Microbiological testing. The entire laboratory and manufacturing facility is as per the Drugs and Cosmetic Act.

      Pharmaceutical Manufacturing Activities as Licensed by the National Drug Authority:

      All the Pharmaceutical Manufacturing Activities are carried out as per WHO-GMP & Schedule–M of the Indian Drugs & Cosmetics Act. The day to day licensing and regulatory activities are controlled by Drugs Control & Licensing Authority, Drug Controller Kolkata, Food & Drug Administration and CDSCO (Central Drug Standard Control Organization), Kolkata, East Zone –India

  • Unit III-Tetradrip Pharma Pvt.Ltd.(Pharma Impex Lab group of Company-Burdwan Plant)
    • Brief Information of the Firm:

      Tetradrip Pharma Private Limitedwas established in the year 2013. It is engaged in manufacturing and marketing of Haemodialysis Solution and Cephalosporin Antibiotics. Tetradrip Pharma Private Limited strives to provide high quality pharmaceuticals that improve the health of the customers. A team of personnel of various disciplines and pharmaceutical experts are working towards to meet the customers’ requirements and objective of continuous improvement in quality. The construction work of this unit was started at January 2016. The whole project was divided into two phases: Phase 1: Haemodialysis Solution Block, Quality Control and Administration Block. Phase 2: Cephalosporin Block to have Cephalosporin dry powder injection. The work of Phase 1 was completed in record time of 13 months and the company applied for the drug license in January 2017. The plant is located at Haldiwhich is outskirts of Burdwan town, approximately 11.0 km from National Highway 2. Burdwan is approximately 100.0 km from Kolkata airport.

      Pharmaceutical Manufacturing Activities:

      It has to be licensed by the Drug Controller, to manufacture formulations for Haemodialysis Solution.Manufacturing License No.: DL-1648-M. The company is also in the process of building a state of art technology to manufacture cephalosporin formulations including cephalosporin dry powder injection and applied for the drug license by the Drug Controller.

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