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Stason Pharmaceuticals, Inc.

 Stason Pharmaceuticals, Inc. Logo

Contact:


Diana Wood
Business Development
Phone #: 949 380-4327
Fax #: 949 380-4345
Email: inquiry@stason.com
Website: www.stasonpharma.com

Address:


11 Morgan
Irvine, CA 92618
USA

Company Description:

Stason is a vertically integrated cGMP contract development organization and offers immediate, delayed release, and fast disintegrating technologies for oral products. We offer both Conventional Operations, & High Containment Operations (capability to handle Category I-IV compounds). Stason provides bench top to commercial manufacturing with facilities throughout the US & Asia.

Additional Information:

Corporate Capabilities PDF: Download

Stason Pharmaceuticals, Inc. deals in the following categories:


Accelerated Stability Studies Analytical Lab 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 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, Creams & Ointments
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, Powders
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, 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 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