Acceleration, LLC - CMOCRO

Drug Delevopment & Delivery

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Acceleration, LLC

Acceleration provides its clients with the comprehensive, current, and customized information related to product development, analytical methods, testing, and marketing of pharmaceuticals and other products. We provide contract testing for all pharmaceutical businesses, large and small, including virtual companies.

Company Contact:

Thomas W. Rosanske, PhD
Phone:

(816) 984-8718
Fax:

(816) 525-1151
Email:

trosanske@accelerationkc.com
Website:

http://www.accelerationkc.com/
Address:

2634 NE HaganLee\'s Summit, Missouri 64064

USA
North America

Service Information
CRO Capabilities

ANALYTICAL

API Type

Controlled Substance Cytotoxic High Potency Drug Nutraceutical OTC Polymer Small Molecule

Sample Type

API Cleaning/Validation Dosage form Intermediate Raw Material

Service Type

Differential Scanning Calorimetry Methods Method Development Method Transfer Method Validation Reference Standard Certification Tests - Dissolution/Disintegration Disintegration Dissolution App. I/II Tests - Impurities/Degradation Forced Degradation Imp./Deg Quantitation Tests - Physical Particulate Matter Physical Testing Tablet Hardness/Friability Tests - Stability Accelerated Stability ICH/Commercial Stability Storage ICH/Commercial Stability Testing Photostability Stability Storage (I/II)Stability Testing (I/II)Tests/Analysis - Other Assay/Potency Chiral Separation/Analysis Comparator Analysis Compendial Testing Content Uniformity Fourier Transform Infrared Analysis Investigative Analysis LCMS Analysis Moisture Molar Extinction Coefficient Determination Residual Solvent Analysis Sample Analysis Thermal Analyses/DSC Thermogravimetric analysis Trace Analysis Tets - Release In-vitro release testing Lot and Batch Release Testing Wet Chemistry

API/BIOLOGICS/REAGENTS

API Development Stage

Discovery GMP clinical GMP commercial Preclinical

API Types

Biologics Peptide

CONSULTANT

Areas of Expertise

Research/Development Analytical API Audits CMC Product Development Quality Assurance Quality Control

FACILITY REGULATORY STATUS

Facility regulatory bodies

Facility subcategories

Inspected Qualified/accredited

FORMULATION/MANUFACTURING

API/Business Sector Types

Controlled Substance Cytotoxic High Potency OTC Small Molecule

Development Stage

GLP/Tox Support Manufacturing GMP Clinical (Phase I/II)ICH Batches

Formulation Type

PACKAGING/FILLING/LABELING

Development Stage

Packaging Filling Services

Clinical Package/Label

PREFORMULATION

Preformulation Services

Accelerated Stability Excipient Compatibility Forced Degradation Studies FTIR Moisture Content Partition Coefficient pH-Rate profiles Physical Properties Pka Solubility Specific Gravity Thermal Analyses/DSC

REGULATORY

Formulation Category

Controlled Substances Cytotoxic Formulations Generics High Potency Drug Formulations Oral

Regulatory Services

SUPPLY CHAIN MANAGEMENT

Supply Chain Services

Distribution Product Storage

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