Acceleration Laboratory Services is an independent, FDA inspected, contract GMP pharmaceutical laboratory.

1. Acceleration Laboratory Services
2634 NE Hagan Rd. • Lee’s Summit, Missouri 64064
816.525.1150 phone • 816.525.1151 fax
www.AccelerationKC.com

2. Acceleration Laboratory Services is an FDA
Quality is Paramount. Service is Superior.
inspected contract drug development and
research organization (CRO) headquartered in the
Kansas City metropolitan area. Our accomplished
associates bring advanced knowledge and
attention to detail — along with solid science and
an analytical perspective — to achieve quality
Quality Services
outcomes at any point during the drug development
process. Acceleration provides comprehensive, current • Drug Products (most dosage forms) • Antimicrobial Effectiveness USP <51> Acceleration Gives…
and customized data and information related to • Battery of Standard Tests • Sterility USP <71> Acceleration helps accelerate your drug
Acceleration serves clients of all sizes in the product development, analytical methods, • Compendial testing (USP, EP, & JP) • Pharmaceutical Water Testing development through:
pharmaceutical, animal health, other life sciences testing and marketing of pharmaceuticals, • Excipients (Vendor Qualification Support)
and food/beverage industries. Acceleration as well as other types of products. We provide • Certificate of Analysis Generation Manufacturing Services Highest Quality
GMP Manufacturing Phase I & II Clinical Supplies • FDA Inspected
offers analytical services at every phase of the contract testing for a variety of life science Stability Testing
• Powder in Capsule • GMP/GLP
development continuum, including evaluation of businesses, large and small, including virtual • Drug Substances
• Powder in Vial • Intensive Laboratory Training
chemistry, safety, and stability through packaging, companies. • Drug Products
• Aliquotting/Subdividing • Intensive SOP Training
labeling, storage and shipment of product. Our • ICH (5°C, 25°C/60% RH, 30°C/65% RH, • Independently Audited
We also provide specialized solutions to
40°C/75% RH) Clinical Packaging/Labeling
end goal is to make sure the product reaching the address your custom needs. Expedience
• ICH Photostability (Options 1 & 2) • Primary - Capsules/Tablets in Bottles
consumer is well characterized and as accurately • Custom Conditions (-20°C, 50°C/75% RH, • We will work with customers to meet
Acceleration focuses on: • Secondary – Packaging, Labeling
evaluated as possible. or per customer needs) • Distribution deadlines
• Analytical Chemistry Services • Special Rush Service
Associates with Experience and Acumen • Temperature Cycling Studies
• Manufacturing Services • Fully Validated Chambers - Monitored 24/7 Storage and Distribution
Clients enjoy a higher level of service with GMP Warehouse – Storage, Inventory, Aliquotting Creative Pricing
• Packaging and Labeling Services • Uninterrupted Power
• Discounts available for volume work
Acceleration associates averaging over 10 • Protocols & Global Distribution
• Storage and Distribution Services • Drug Substances • Discounts available for guaranteed work
years experience in the industry. All Acceleration • Submission Ready Reports
• Drug Products (in primary package and kits) • FTE contracts available
associates are degreed professionals. With an • Customized Solutions Additional Capabilities
• Excipients
associate turnover rate far lower than most contract • Controlled Substances
research organizations, customers enjoy stability Analytical Chemistry (DEA Schedules I – V)
• Analytical Method Development/ • Potent Compound Handling
and consistency, which directly affects quality.
Validation/Transfer • GMP Routine Sample Testing
At Acceleration Laboratory Services, our first and • Assay, Related Impurities, Chiral • Reference Standard Subdivision
and Distribution
foremost principle is “people first.” We are founded • Forced Degradation Studies
• Compatibility Studies
on that principle and we remain dedicated to the • Residual Solvents
• Cleaning Validation
ideal that people matter most. Our associates are • HPLC, UPLC, GC, Dissolution, LC/MS, IR, KF,
• GLP Dosing Solution Preparation
etc.
both technically astute and customer oriented; they • GLP Dosing Solution Analysis
• Reference Standard Qualification • GLP Stability Studies
understand that quality is not measured just in the
• Method Remediation or Optimization • CMC Support
accuracy of results. A true quality product must be • Development/Validation Report • CMC Consulting
timely, accurate, and meet or exceed our customer’s (appropriate for “Drop-In” to Regulatory • Package Integrity
expectations. Filing)
Our objective is to make each proposal – every Microbiology Testing
project – a successful venture for both our customers Release Testing • Bacterial Endotoxin USP <85>
• Drug Substances • Bioburden/Microbial Limits USP
and ourselves.
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