Infrastructure and Manufacturing Facility


Mercury manufacturing facilities is designed, equipped and operated to deliver high quality products within defined cost and delivery schedules. These manufacturing facilities have flexibility to operate in various dosage forms and wide range of batch sizes.

Mercury operates three formulation manufacturing facilities, of which two are located at Jarod (Nr. Waghodia, Dist. Baroda.) & rest at Baroda.




  • Total plant area (Tablet) - 17,653 sq. ft.
  • Total plant area (Liquid) - 15,597 sq. ft.
  • Total plant area (Injection) - 23,024 sq. ft.
  • Our New upcoming plant near jarod, designed & well equipped with respect to MHRA Guidelines having - 34,444 sq. ft. area.



Global scale production capacity :

Tablets : 60 million tablets per month

Liquid : 1.5 million bottles per month

Injection : 1.5 million ampoules & 0.5 million vials per month

Research & Development


Primary focus area in formulation development includes:
  • Developing new drug formulations for existing products for life cycle management
  • Improving processes for existing formulation
  • Taking trial batch for new products
  • Improving existing product quality & shelf life
  • Manage cost efficiency, consistency of process in manufacturing environment.

Quality embodies the spirit of the company.
We believe that quality is the mainstay of competitiveness.
We thus constantly create an environment of Quality and Compliance in line with the global best practices.

Quality Policy


    At Mercury Laboratories, we believe that customer satisfaction, in terms of quality, delivery and after sales service, is our first and foremost responsibility.

    We are committed to constantly improve the quality standards of our product and services by implementation of cGMP, up-gradation in technology; imparting training to effectively adapt to newer technologies and high standard.

    Our personal credo is that each individual is responsible for the quality of his/her work and shall continuously strive to attain excellence in the same.

    We treat each other fairly, with trust and respect, in an environment that fosters involvement, open communication and teamwork.


    The company has state of the art manufacturing facilities conforming to the most stringent international GMP norms vis-a-vis WHO-GMP, WHO, ISO 9001 Spread Over Hundred Acres Of Land.


We have a manufacturing facility approved by Ghana, Sri Lanka, Nigeria.

Our Quality Assurance systems are designed, which individually or collectively influence the quality of the product. Regular control of system functioning to Incorporates Good Manufacturing Practice plus other factors such as product design and development. The systems have been designed to meet and be compliant to global Quality Systems.



Quality Management System :

The company believes in total quality management system and is constantly upgrading standards of specifications of its products. The quality policy states as under: The policy of Mercury Laboratories Limited is to ensure that the quality of the products satisfies the safety, efficacy and other requirements of customer and society according to current good manufacturing and laboratory practices.

  • Quality has been the prime consideration in recruitment of manpower.
  • For further strengthening the system, following activities are carried out
  • The In-house training program covers all relevant aspects of CGMP.
  • Control of input materials by testing them as per our well-defined specifications controls / control procedures. Like wise well defined specifications, test and release procedures are followed for semi finished and finished products exit. Production as well as Quality Assurance, monitors quality by carrying out in process testing and controls during various stages of manufacturing.
  • Standard operating procedures are available for different operations. Products are manufactured as per procedures given in batch manufacturing records and recorded accordingly.
  • Standard validation/calibration protocol is adhered to for validation of all critical equipments/processes/instruments.
  • Master formula records, which are prepared for individual products, are adhered to in batch manufacturing & testing processes.
  • Maintenance history records are maintained for critical instruments and equipments to ensure proper preventive maintenance.
  • The assessment of effectiveness of Quality management system is done by periodic self inspections covering all aspect of factory operations and most importantly.
  • Incoming material Quality
  • Product Quality
  • Compliance with systems / document control
  • Customer complaints
  • Corrective action to avoid non-conformity
  • Out of Specifications (OOS)
  • Internal Quality Audits




Quality embodies the spirit of the company.

We believe that quality is the mainstay of competitiveness. We thus constantly create an environment of Quality and Compliance in line with the global best practices.






Our Facility Complies With GMP

  • Formulation & Development
  • Raw Material Procurement & Manufacturing
  • Analytical & Process Development / Validation
  • Stability As Per ICH, Storage & Testing
  • Quality Control & Release

Our Quality Control department is well equipped with High quality & latest technological instruments like HPLC, Fourier-Transform Infrared spectrophotometer, Photofluorometer, Dissolution apparatus, Karl-Fisher Instrument, UV-Visible Spectrophotometer.



Our Formulation & Development set up :

Primary focus area in formulation development includes :

  • Developing new drug formulations for existing Products for life cycle management
  • Improving processes for existing formulation
  • Taking trial batch for new products.
  • Improving existing product quality & shelf life.
  • Manage cost efficiency, consistency of process in manufacturing environment.