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Batavia Exports
International

Contract Manufacturing,

Private label manufactuing, toll manufacturing

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.  
- Manufacturing of tablets, capsules, sry syrups, dry powder injectibles  
- UK MHRA, EU GMP, Germand FDA, TGA approved manufacturing site  
- Over 12 associtaed manufacturing plants  
- Products handeled includes : Betalactum and Non Betalactum products  
- Dedicated facilities for cephalosporin tablets, capsules, dry powder injectibles  
- Ideal for site Variations for European Union  
- Excellent environment, with cheaper labour and capital costs in India, availability of Active Ingredients locally  
- Competitive pricing and ample capacity for assured deliveries  
- Supply management backed by supply of quality active and inactive ingredients  
Regulatory support  
a.Site Variation  
b. API Variation.  
 
Toll Manufacturing an Integrated approach  
- 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.  
- 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 .  
- Batch Release in the EU with our other associates if required  
 

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.

 
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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