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Stason Pharmaceuticals, Inc.
Irvine, CA, 92618 USA
VP Business Development
Stason Pharmaceuticals, Inc. is a fully-integrated cGMP contract development organization providing complete turn-key drug development services for oral products. We offer services for both non-High Containment and High Containment Products. Stason offers a range of services for New Chemical Entities, generics, and upgrades to existing formulations, and provides development and manufacturing services in its FDA inspected facilities. We currently produce finished products at all scales through to commercial scale.
Contract Services Directory Accelerated Stability Studies Analytical Laboratory Services Analytical Methods Development Analytical Validation Studies Assay Development Auditing Bioanalytical Analysis LC/MS/MS Blending cGMP Synthesis Chemical Analysis Chromatographic Analysis, LC/GC Clean Room Services Clinical Analysis Clinical Trials, Phase I Clinical Trials, Phase II Clinical Trials, Phase III Clinical Trials, Phase IV CMC (Chemistry, Manfacturing & Controls) Coating & Lamination Consulting Consulting, Regulatory Contract Development and Manufacturing Organization (CDMO) Contract Manufacturing Custom Manufacturing Custom Protocols Custom Synthesis Dissolution Testing Distribution, Commercial DMF Establishment / Maintenance Documentation Support Services Dosage Form Development Drug Delivery Systems Drug Design Drug Development Services Encapsulation Excipients Filling, Capsule Forced Degradation Studies Formulation Development Formulation Services GLP Auditing GMP Auditing Granulation In Vitro Testing IND/NDA Submissions Lot Release Testing Lyophilization Machinery Design and Construction Manufacturing, API Manufacturing, Bioequivalence Manufacturing, Capsules Manufacturing, Clinical Trials Supply Manufacturing, Consultants Manufacturing, Controlled Substances Manufacturing, Cytoxic & High Potency Compounds Manufacturing, Dose Form, Non-Sterile Manufacturing, Dose Form, Sterile Manufacturing, Ethical Manufacturing, Gels Manufacturing, Generics Manufacturing, High Containment Operations Manufacturing, Oral Drug Delivery Manufacturing, OTC Manufacturing, Solid Dosage Manufacturing, Solutions & Suspensions Manufacturing, Sustained Release Manufacturing, Tablets Manufacturing, Topicals Materials Analysis Methods Development Methods Validation Microencapsulation Mixing & Blending Nonclinical Research Organic Synthesis Packaging, Blister Packaging, Capsules Packaging, Certification Packaging, Clinical Trial Materials Packaging, Clinical Trials Packaging, Compliance Packaging, Consultants Packaging, Creams & Ointments Packaging, Design & Testing Packaging, Development Packaging, Form/Fill/Seal Packaging, Labels Packaging, OTC Packaging, Powders Packaging, Samples Packaging, Services, Other Packaging, Solid Dosage Packaging, Unit Dosage Physical Testing Pilot-Scale Filling Preclinical Study Design Preclinical Testing Preclinical Testing Formulations Preformulation Process Development/Scale-Up Services Process R&D Process Validation Studies QA/QC Quality Control Testing R&D Services Raw Materials Analysis Regulatory Affairs Consultants Scale-Up Screening, Classifying Shipping Size Reduction Stability Studies Stability, ICH Sterilization Storage Supplier, Excipients Supplier, Fine Chemicals Supplier, Raw Materials Sustained Release Delivery Systems Tablet Coating Technology Transfer Torque Testing Training Training: cGMP/HPB/FDA Compliance Training: Process Validation Training: Safety UV-VIS Spectrophotometer Analysis Validation, Clinical Validation, Equipment Cleaning Validation, Manufacturing Validation, Services Wet Chemical Analysis
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