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Stallion Laboratories Private Limited

Ahmedabad, Gujarat

IndiaMART Member Since: 2008
Products [22]
Phone: +(91)-(79)-26441993

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A WHO-GMP, ISO-9001:2000 certified company; Stallion Laboratories serves its healthcare commitment with a wide range of Pharmaceutical Formulations and Complimentary & alternative medicines. Today Stallion Laboratories is amongst the fastest growing pharmaceutical companies in India.


Assisted by host of experienced professionals and given the current pace of activities with constant efforts for improvement and innovation, Stallion Laboratories is poised to make its presence felt globally.


The Stallion Laboratories began its corporate journey as a Pharmaceutical Agency & Manufacturer in the late Eighties. It has a state of the art facility located in the GIDC Estate in Ahmedabad, Gujarat province of India.


The whole edifice has been constructed by FDCA-approved technicians and engineers. The manufacturing facility and laboratory is in tandem with the highest standards of medicinal formulation environment. In fact it is this stringent quality orientation, that has availed us the coveted WHO's Good Manufacturing Practices certificate. Our operational activities too have an equally professional approach, and our certification by ISO 9001:2000, is a testimony of the same.


Stallion Laboratories Pvt. Ltd. (SLPL) obtained the FDCA license for state of the art facility for Oral Liquid Manufacturing & Quality Control in 1989, with simultaneous arrangement for sophisticated facility for manufacturing Tablets & Capsules.


In 1995, the company expanded its existing infrastructure and its unit in another 22,500 sq. feet land with ultra-modern and most advanced machinery. Company has changed its all manual and semiautomatic machinery to fully automatic machinery complying with WHO-GMP standards. A new, full-fledged laboratory with microbiology section was established, and equipment conforming to WHO-GMP norms like GC, HPLC, IR spectroscopy, UV visible spectrophotometer etc. were installed.


In 1996, Stallion Laboratories secured the license for manufacturing Betalactum & General Capsules from the FDCA. In the same year, the FDCA approval to manufacture Children's & General Coated and Uncoated Tablets also came its way.


Today, the company produces a wide range of Pharmaceutical Formulations and Complimentary & alternative medicines, which are preferred by Medical Practitioners and OTC customers for their proven efficacy and reliability. The company has its reputed presence not only in the domestic market, but also in potential international markets too.


The urge to grow, and the commitment to provide more and more integrated Medicare solutions, will continue to shape up our future, so is the reason Development at Stallion is a continuous process.

Quality Policy / Processes

Quality Policy / Processes

 

Our focus on R&D and adherence to stringent quality control makes all the products of Stallion a world class benchmark. The company endeavors to meet established and emerging international standards at the qualitative level, because it knows once a qualitative parity is established, quantitative growth will follow on its own.

The laboratories and plants at Stallion are characterized by stringent quality assessment & control systems, operative at every stage of production.

Installation of dedicated Air Handling Units (AHUs) at every stage of production to prevent air/particulate contamination is the key feature of the facility. Calibration and validation of respective equipments and process' are carried out as per Standard Operating Procedures (SOPs).

Quality monitoring with religious zeal translates the chief methodologies such as: complete documentation of the production process' where  each analysis, and inference is recorded in the Departmental Procedure Manuals, for future reference. Currently, this Documentation Methodology is applied to product & process specifications, batch manufacturing records, analytical methods and quality analysis procedures.

Uniformity of the finished product across all the batches is the testimony to the fact how crucially the BMRs are prepared and followed as a guideline.

This process enables the company to effectively control the quality of the entire manufacturing process. Also, to keep watch over the efficiency and motivational levels of its employees.

Finished products are dispatched for distribution after confirmative approval of Quality. The Representative samples of each batch are retained for Various tests as well as real life stability studies, while the product is in the market for the entire shelf life period.

 


Fact Sheet
Nature of Business:Manufacturer


Contact Details

 
Company Name:
Stallion Laboratories Private Limited
Contact Person: Mr. Manager
Telephone: +(91)-(79)-26441993
Fax No: +(91)-(79)-26560543
Address: 817, 8th Floor, Devpath, C.G. Road, Ahmedabad, Gujarat - 380006 (India)

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