EXCITE PHARMA SERVICES, LLC
Excite Pharma is a leading provider of CDMO and CRO services, specializing in small-scale aseptic manufacturing, analytical chemistry, and drug development. Committed to patient safety and high-quality service, the company serves pharmaceutical and biopharmaceutical clients with a focus on smaller batch projects, offering innovative solutions and comprehensive support from formulation to commercial manufacturing.
Industries
Nr. of Employees
small (1-50)
EXCITE PHARMA SERVICES, LLC
Lees Summit, Missouri, United States, North America
Services
Aseptic filling and cGMP sterile manufacturing
Contract aseptic filling and sterile manufacturing for clinical and small commercial batches, supporting vial, syringe and ophthalmic formats across multiple fill lines and hand‑fill operations.
Analytical chemistry services (CMC support)
Comprehensive analytical support including method development, validation, transfers, identification, assay and impurity testing to support CMC documentation.
GMP release testing / batch analysis
In-house batch release testing for drug substances, drug products and excipients per ICH/USP guidance, including chemical, physical and microbiological endpoints.
Method development, validation and transfer
Analytical method development and validation for APIs, drug products and biological matrices, and transfer of validated methods to client sites or partners.
Stability programs
Design and conduct of stability studies (long-term, accelerated, refrigerated, frozen and photostability) following ICH Q1E to establish shelf-life and storage conditions.
Residual solvent and VOC analysis
Residual solvent testing by static headspace GC/FID and GC/MS per USP guidance, customized to process-specific solvent profiles.
Aseptic filling and cGMP sterile manufacturing
Contract aseptic filling and sterile manufacturing for clinical and small commercial batches, supporting vial, syringe and ophthalmic formats across multiple fill lines and hand‑fill operations.
Analytical chemistry services (CMC support)
Comprehensive analytical support including method development, validation, transfers, identification, assay and impurity testing to support CMC documentation.
GMP release testing / batch analysis
In-house batch release testing for drug substances, drug products and excipients per ICH/USP guidance, including chemical, physical and microbiological endpoints.
Method development, validation and transfer
Analytical method development and validation for APIs, drug products and biological matrices, and transfer of validated methods to client sites or partners.
Stability programs
Design and conduct of stability studies (long-term, accelerated, refrigerated, frozen and photostability) following ICH Q1E to establish shelf-life and storage conditions.
Residual solvent and VOC analysis
Residual solvent testing by static headspace GC/FID and GC/MS per USP guidance, customized to process-specific solvent profiles.
Expertise Areas
- Aseptic small-batch and clinical manufacturing
- Analytical chemistry and method development
- Stability program design and execution
- Release and batch testing for APIs and drug products
Key Technologies
- HPLC / UPLC
- Gas chromatography (GC) and GC‑MS
- Static headspace GC‑FID
- ICP‑MS (metals analysis)