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About Us
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Management Team
Solution & Service
API & Intermediates CDMO Service
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Analytical Service
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Drug Product Analysis Service
API & Intermediates CDMO Service
Process Development Service
Synthesis Route Design
Development & Optimization
QbD Study
Process Validation
Manufacturing Service
Process Development Service
Drug Product CDMO Service
Pre-clinical Drug Product R&D Service
Salt and Polymorph Screening
NCE Characterization
Pre Clinical Formulation Development
Clinical Drug Product R&D Services
Clinical and Commercial Drug Product Manufacturing Services
Global Regulatory Submission Services
Analytical Service
API Analysis Service
Pre-formulation Analysis Service
Drug Product Analysis Service
Stability Study
Data Integrity
Support
Global CMC Filing
Project Management
Product Lifecycle Management
For more information about
"Drug Product Analysis Service",
please contact our team.
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Drug Product Analysis Service
Impurity and assay method, content uniformity method, and blend uniformity method developments, validations, and transfers for various dosage forms
Discriminative dissolution method developments, validations, and transfers
Provide IND/NDA ready-for-filing readiness, method development reports, method monographs, and method validation reports per ICH guidelines