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FLEMING LABORATORIES LIMITED

About us 

Fleming Laboratories Limited commenced operations in 1994 with the manufacturing of Cinnarizine. Today it is not only one of the major producers of this product in the world, but is now manufacturing several other niche and of beat API'S with 2 GMP compliance facilities. A third USFDA compliant facility is now underway. Fleming is looking at making its mark in the regulated markets.

Fleming is strongly committed to protection of the environment & has a comprehensive pollution control strategy in place. This will ensure that ISO 14001 certification is released within a few months as well as the company achieving its zero effluent discharge goal.

An excellent HRD & employee welfare system is designed to ensure a highly realized competent GMP trained work force by a very well controlled attrition at the tower levels.

The IP department of our R&D focuses on delivering non-infringing process and Fleming has already filed several Patent applications.

Its Regulatory department has completed several DMF's and is appreciated by discerning customers for the quality of its documentation and response to its technical queries.

Research and Development

In our dedicated Research an Development cum pilot plant we do scale up operations and also custom manufacture of high value and low products ranging from 1-20 kg.

Our QA cell comprising a dedicated team of managers and executives ensures tight control on QA systems, as well as the reliability of its QC functioning.

The instrumentation department of QC is well equipped with the latest HPLC's and GCS as well as UV, Polarometer etc.


Contract Research and Manufacturing

Contract Research (CR)

Well equipped R&D centre cum pilot plant for scale with qualified & experienced Scientists Fully equipped Analytical Laboratory Separate cell for IP (Intellectual Property) Issues Maintenance of confidentiality Customs synthesis of high value products Development of alternate patent non-infringing processes Competence to provide Dossiers/Tech. Pack along the product Development


Contract Manufacturing (CM)

  • WHO GMP Compliant

  • Plant designed to meet USFDA & cGMP

  • Batch capacities from 1-10 kg

  • Manufacturing of Bio - Batches of up to 5 kg

  • Competence to provide Dossiers/Tech pack along with the development batches

 

  

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