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• TOSCO Pharmachem Pvt. Ltd., is committed to manufactureActive Pharmaceuticals and it’s Intermediates to meetpredetermined standards as specified by various National andInternational regulatory guidelines.
• We are also committed to implement all the required cGMPnorms as per schedule “M”, WHO TRS, ICH guidelines and alsoallied guidelines for the manufacture purity, Identity, Strength,Safe, Efficiency and Quality API’s and its intermediates for thebenefit of customer at affordable prices in health care sector.
• We are also committed in continuous improvement byimplementing Total Quality management System (TQM), GoodLaboratory Practice (GLP), GOOD Engineering Practices (GEP)and Good Storage Practice (GSP) at our site to meet thecustomer and regulatory requirements.
Customer Centricity
Continuous Improvement
Premium Quality Products
Cutting Edge Solutions
QUALITY POLICY
QUALITY POLICY
cGMP Manufacturing» API and Advanced Intermediates
» Fine Chemicals
Process R&D» Process Development/ Optimization &Validations
» Tech transfers from bench scale to Commercial plant level
Custom Synthesis» Advanced Intermediates» Key Starting Materials
SERVICES
ACCREDITATIONS
ACCREDITATIONS
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