Quality Control
ESHYASI PHARMA LTD. a team of Technical People who have experience of one to two decades in Regulatory Affairs, Quality Assurance, Quality Control, Analytical Development and R & D. We understand need of Regulatory affairs and it has vital role in the pharmaceutical business. If no Regulatory Control, there is no pharmaceutical business. Many pharmaceutical companies in India and overseas have started outsourcing such services rather than creating own division, which will help them to reduce cost as well as concentrate other areas.
Our services:
QC FUNCTION
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Specifications & Analytical procedure development
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Stability study as per ICH guidelines
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Analytical services
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Documentation
ADL FUNCTION
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Analytical Method Development & Documentation
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Analytical Method Validation & Documentation
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Forced Degradation / Stress studies & Documentation
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Technology Transfer
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Process Development & Report Development
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Characterization / structural Elucidation
QA FUNCTIONS
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VMP preparation
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SOP Development & Trainings
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Facility Qualification
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Equipment Qualification
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Facility Design as per GMP norms
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GMP Trainings & Documentation
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Site Master File
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Quality Manual
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GMP Documentation
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Process Validation & Documentation
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Cleaning validation & Documentation
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Vendor Development
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Third party Audits
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Master Formula / Batch Record Development
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Quality system development
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Period Review of Quality systems