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)
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WHO GMP Compliant
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Plant designed to meet USFDA & cGMP
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Batch capacities from 1-10 kg
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Manufacturing of Bio - Batches of up to 5 kg
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Competence to provide Dossiers/Tech pack
along with the development batches
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