| In a competitive
market environment outsourcing is in evitable and toll manufacturing
an essential part of the pharmaceutical industry. India is being recognized
as one of the growing hunbs for quaity contract manufacturing of pharmaceuticals.
We offer toll manufacturing services, manufacturing is done at GMP
certified manufacturing facilities of our parters. |
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Manufacturing of tablets, capsules, sry syrups, dry powder injectibles |
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UK MHRA, EU GMP, Germand FDA, TGA approved manufacturing site |
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Over 12 associtaed manufacturing plants |
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Products handeled includes : Betalactum and Non Betalactum products |
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Dedicated facilities for cephalosporin tablets, capsules, dry powder
injectibles |
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Ideal for site Variations for European Union |
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Excellent environment, with cheaper labour and capital costs in India,
availability of Active Ingredients locally |
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Competitive pricing and ample capacity for assured deliveries |
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Supply management backed by supply of quality active and inactive
ingredients |
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| Regulatory
support |
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| a.Site Variation |
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| b. API Variation. |
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| Toll
Manufacturing an Integrated approach |
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Supply of Active Ingredients with cmopltee documnetation with regulatory
approvals as per Eu directives including EU CTD DMF, COS from EDQM
and plant approvals for GMP compliance. |
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Production of formulations at the most suitable manufacturing facility
with a view of backward integration whereever possible fro API manufacturing
done by the smae organization . |
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Batch Release in the EU with our other associates if required |
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Our local presence
allows us a substantial benefit including Raw Material supply with
GMP complaince and competitive pricing., which has an important
role in termsof immediate and prompt dispatches. With in house regulatory
support, every project is deligently handled with the right API
source and the right manufacturing facility. Every manufacturing
platn has its own uniqueness and are made as " stateof the
art " world calss high qualtiy manufacturing sites desigend
to meet the best standards in the world. MHRA, EU GMP approvals
and GMP complainces are a testimony to thist fact.
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| Production for
formulations is conducted in accordance with EU Guidelines and directives
and all facilities confirm to GMP guideliens of the E.U |
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