Tel No. +91-9039935888

About Us

showcase image

Our Company

We are a C-GMP Certified Company incorporated in 2007 is today one of the leading and most reliable manufacturer of small volume parenterals especially expertise in Sterile Water for Injections (SWFI), Sterile Water for Reconstitution of dry syrup (SWFR) and Sodium Chloride Injection (SALINE), sodium bicarbonate injections and dextrose injections, employing Aseptic form-Fill-Seal (FFS) technology with well integrated operations. It is spread over an area of approx. 25.000 sq. ft, strategically located at central India in Jabalpur, Madhya Pradesh . The unit is duly audited and approved by several government food and drug authorities, leading pharmaceutical companies and exporters for their regular supplies.

Our Vision and Mission

To be a leading player in the field of small volume healthcare products by manufacturing and supplying high quality parenteral products and thus contribute to the wellbeing of humankind. We check the quality of our products,validate the manufacturing process to ensure standard products.

Our mission is to become the most valued Pharma partner to the World Pharma fraternity by continuously researching, developing and manufacturing a wide range of pharmaceutical products in coming future that comply with the highest regulatory standards.


We apply Continuous Exploration which is the the method of frequently exploring the market and user needs, and shaping a Vision, Roadmap, and set of options that address those needs. It’s the primary component within the four-part Continuous Delivery, preceding Continuous Integration Continuous deployment, and unleash on Demand.
We practice quality management ensures that our product or service is consistent. It has four main components: quality planning, quality assurance, quality control and quality improvement. Quality management is focused not only on product and service quality, but also on the means to achieve it. Quality management, therefore, uses quality assurance and control of processes as well as products to achieve more consistent quality.
In our company we ensure appreciation, strength and communication which are the key elements of practicing team work in any organization. Our staff is highly educated, learned, trained and concerned with the each other. We all know that Teamwork is the collaborative effort of a team to achieve a common goal or to complete a task in the most effective and efficient way.
We are bound to produce the product with high quality which complies in all tests and measurements. Cost effectiveness is the need of pharma industry. We ensure the production is cost effective with the quality that ensures product reliable using innovation and technology.
Continuous exploration & development of new products & processes|Laying emphasis on cost effectiveness|Maintaining effective Quality Management System|Imparting training to all involved on a continuous basis|Team work and active participation all around|Foster mutually beneficial relations with all our business partners|Manage our operations with high concern for safety and environment.

Our Expertise

Manufacturing Small Volume Parenterals
40% Complete (success)
40% Complete (success)
Trading & wholesale
40% Complete (success)
Client Satisfaction
40% Complete (success)


We are the manufacturer and wholesalers of Small volume Parenterals pharma products specially expertise in WFI | SWFI | SWFR | SALINE | Dextrose Inj.


Sterile Water For Injection, IP/BP/USP, a sterile version of water for injection which is used for making solutions that will be given by injection.


Sterile Water For Reconstitution, IP/BP/USP, of dry syrup, a sterile version of water which is used for making oral solutions specially antibiotics.


Sodium Chloride Injection, IP/BP/USP is a sterile, nonpyrogenic solution for fluid and electrolyte replenishment in single dose containers for intravenous administration. It contains no antimicrobial agents.


Dextrose (hydrous dextrose) Injection, IP/BP/USP is a sterile, nonpyrogenic solution for fluid replenishment and caloric supply in single dose containers for intravenous administration.

Manufaturing facility

Innovation in FFS Technology: Form Fill Seal (FFS) Bagging Innovation

At Deo Gratias Parenteral, we have designed and developed a unique form-fill-seal procedure This moulds polyethylene polymer containers, fills them aseptically and performs hermetic sealing of the containers as part of a single, sequential operation. The FFS (FORM FILL SEAL) aseptic machine is equipped with an integrated clean room modular design; here we maintain class conditions, prevent cross-contamination and avoid mix-ups. Man and material flow is designed to be linear and easy to follow. Filling and sealing processes are performed in Class 100 conditions that are achieved through the validated use of Laminar Air Flow units, all the processes fulfill GMP norms.

Key features includes:

  • Hands free Fully Automatic Manufacturing Process.
  • A.F.F.S for Terminal Sterilization.
  • Pressure vessels, Solution preparation tanks from reputed suppliers.
  • Vacuum Leak Test Machine.
  • Multi Column Distillation Plant.
  • Post sterilization with super heater sterlizer.
  • On Line Labeling Machine.
  • On Line visual inspection conveyors for extra care.
  • Distilled water tank of suitable capacity.
  • Fast-track project delivery through truly standardised product.
  • Automated PLC control minimises operator involvement.
  • Guaranteed microbial compliance through regular hot water at 85°C.
  • Designed, manufactured and validated to CGMP.
  • Designed unique efficiently and reliably ensures product quality.

About Images

About Images


Innovation in FFS Technology: Ensuring a supply of pyrogen-free water

Pyrogens can be described as all substances that induce fever in humans or certain test animals within a limited effective period when applied parenterally in minute quantities. They can be regarded as relatively thermally stable and insensitive to pH changes.

There can be several sources of pyrogens in parenteral and medical device products. Usual sources include the water used as the solvent or in the processing and packaging components, as well as the chemicals, raw materials or equipment used in the preparation of the product. Good practice would include control of the microbiological and endotoxin levels of contamination in the potential sources.

At our plant, Purified Pyrogen Free water for injection is being produced using a filteration chain of Chlorination, Sand Filter, Softner , Ultra Filtration (UF) Millipore, Double Pass Reverse Osmosis(RO), Continuous Electro-Deionisation (CEDI) and UV Light treatment which helps to remove most particle, pyrogens, heavy minerals, colloids, microorganisms and also kills microbes.Further, this purified water undergoes Multi-Column Distillation removing Endotoxins. Finally WFI is filtered through 0.1u Filter.Produces high grade purified water.

About Images