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Formulation

The designing of finished dosage facility need special precautions for cGMP, Quality, Contaminations control, Regulatory compliances and Safety.

GBP is involved in designing of Formulation Facilities right from the conceptual design stage, capacity planning, equipment selection, FAT, SAT  to final Qualification and validation of equipment and  facility. We has separate team of experts and projects to execute various formulation facilities of different forms like Tablets, Injectable, Eye and Nasal Drops, Semi-Solids, Ointments and Creams.
Our expertise are special taken care for designing of  US FDA, EU GMP, UK MHRA, Health Canada, Brazil ANVISA,   Australian TGA, WHO facilities.

GBP team are capable for setting up below facilities:

  • Capsules
  • Tablets
  • Dry Powders (In Sachets & Bottles)
  • Liquid Syrups & Suspensions
  • Liquids Injectable in Vials and Ampoules
  • Liquids Injectable in Pre-filled Syringes, Cartridges
  • Nasal Sprays
  • Nebulizers
  • Ointment (Sterile & Non-Sterile)
  • Creams & Lotions
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