Infrastructure & Facilities

Infrastructure & Facilities

Contract Manufacturing

We have gained expertise in catering to contract manufacturing . We have our business tie ups with big medical houses. We manufacture pharmaceutical products catering to their specific needs. Our team of experts take the client''s brief carefully and also under much precisely deliver products to our clients.

Research & Development

We have  well-qualified scientist from different fields like pharmaceutical sciences, microbiology, chemistry, and medical sciences are a part of the organization & new techniques of manufacturing to enhance the efficacy, stability & safety of medicinal products.

Infrastructure

We have possessed the state of art infrastructural facilities that are in compliance with WHO-GMP consisting of four factories:

The parent plant, which is a modern structure, built on an area of 138,000 sq. ft The second facility has a built up area of around 27,000 sq. ft The 3rd plant is under renovation The 4th manufacturing unit is under construction

Machines

A trusted name in the pharmaceutical industry, Health Biotech Limited maintains its quality standards via its well maintained machines. Health Biotech Limited is well equipped with latest machines that are based on the GMP model. The well maintained and efficient machinery is required for manufacturing our wide range of products. The further details of the machines are given below:

Liquid Section- Machines for automatic washing, filling, sealing and labeling are installed in the facility. The automatic liquid manufacturing plant has a capacity 3,000 ltr.
Ointment Section- The plant has a capacity 500 kg. The unit also has ointment filling, sealing and coding machine.
Capsule Section- This unit is equipped with double cone blender, vibro shifter, semi-automatic capsule filing machine, with vacuum pump and change parts.
Syrup Section- This section comprises of semi-automatic jet washing machine, automatic single head auger type powder filing machine with turn table, semi-automatic RoPP cap sealing machine, automatic labeling machine.
Liquid/Dry Injection & Oncology Injection- (Dry & Lyophilized)- The machines for Liquid/Dry Injection installed in the facility includes automatic washing, filing, sealing, inspection and labeling machine, washing 6 Head Filing, 4 Head Filing, Membrane Filter 0.22 micron, 0.45 micron, 1.2 micron & 0.8 micron. The liquid manufacturing tanks have varying capacity of 1000 ltr., 500 ltr., 250 ltr. & 100 ltr, filter vessel, filter holder, membrane filter 0.22 micron, 0.45 micron, 1.2 micron & 0.8 micron. The range of filling machines includes pre-filled syringe machine, lyophilized machine (capacity 12.5 ltr) and Single Head Filing machine. The facility also has Vials/Ampoules transferring trolley, Autoclave, DHS, Crates, Filtration Vessels 25 lts., 10 ltr., 5 ltr. Mixing Tanks.,
Injectable & Ophthalmic Section- This section comprises of Sterile Filing Vessels, Water Storage Tanks, Autoclave, Bung Washing, Laminar Flow (Vertical) Pass Box, Sampling Booths, Dispensing Booths and Air Curtains.


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Company Video

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Company Video

Company Video - Health Biotech Ltd. Health Biotech Limited ( HBL) is one of India's leading pharmaceutical company offering a broad portfolio of finished pharmaceutical formulation. Established in the year 2001, the company manufactures and exports finished pharmaceutical formulation in forms such as Injectable, Tablets, Capsules, Powders, Dry Syrups, Eye / Ear / Nasal Drops, Ointments & Creams.
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Biopharmaceuticals

About:

Company Profile

Biopharmaceuticals

Pharmaceutical Development & Manufacturing

We supports cGMP finish formulation development/product manufacturing with sterile fill and finish, with separate process development laboratory, filling, lyophilization and finish to support production of biopharmaceuticals. Health Biotech Research Centre''s (HBRC''s) scientists use Quality-By-Design (QbD) tools at early as well as late stages of formulation development. Use of Design of experiments (DOE) along with risk assessment strategies helps us to design our experimental plan which is scientifically valid and targeted for completion within our delivery timelines.Whether you are seeking a new formulation, involved in life-cycle management, manufacturing process improvement, or transferring manufacturing to a new site, HBRC’s scientists at Health Biotech Limited can meet your needs.

Contract Process Development Services
  • Process Development for small molecule, injectables and biologics
  • Laboratory scale, pilot scale, cGMP clinical trial materials and cGMP commercial scale
  • Process optimization
  • Technology transfers
Formulation Development
Services offered are as follow:
  • Formulation development for injectable and lyophilized products (clinical to commercial)
  • Process development, optimization and upstream / downstream processing
  • Lab & pilot scale process development
  • Test batches manufacturing for stability studies, test and analysis
  • Clinical packaging & labeling
HBRC has team of expert scientist with rich experience in biotechnology, pharmaceuticals and nanobiotechnology, synchronized for successful development of technology and finish formulations. HBRC''s scientists have extensive multinational expertise developing formulations for conventional and specialized dosage forms, including sustained (SR) & modified release (MR) solids, liquids, and injectables.
Pharmaceutical finished formulation are developed keeping in view product stability, compatibility and patient compliance in custamarized way following Quality by Design (QBD) approach. All of the formulation are designed and developed for techno-economical feasibility and commercialization success. Before prototype development exhaustive pre-formulation studies are performed for characterization of the Active Pharmaceutical Ingredient (API) with excipients. It eliminates potential formulation, manufacturing, scale up, and instability issues. All of the quality and regulatory approval factors are considered at each stage of formulation development for successful commercialization.
Quality by Design (QBD) Program
  • Define Target Product Profile (TPP)
  • Critical Quality Attributes (CQAs) are determined
  • Extensive theoretical and literature survey
  • Risk assessment
  • Control strategy for sensitive products (moisture/oxidation)
  • Lyophilization cycle (recipie) standardization
Biopharmaceutical Analysis

We offers excellent analytical services biopharmaceutical products to support your development and marketed-product needs. We are equipped with state- of-the art analytical equipment required for routine testing, complete characterization of biopharmaceuticals. Our experienced staff possesses an in-depth understanding and regulatory knowledge. We provide quality services and data at affordable cost.

Project Management
HBRC''s experienced project managers are pharmaceutical scientists, life scientist and biotechnologist. In coordination with manufacturing staff they are capable of ensuring your project timelines and expectations. They takes the lead on your development project, from pre-formulation, drug formulation development to clinical trial material (CTM) manufacture - keeping you informed every step of the way.
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Address

S.C.O. 162-164,
Indian Airlines Building, Top Floor,
Sector - 34 Block A

Chandigarh - 160022, India

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