• 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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