Avomeen Analytical Services
Toll-Free: (800) 930-5450
F: (800) 930-5479
E: scientist@avomeen.com
W: www.avomeen.com/pharma

 

Full-Service cGMP Analytical Testing & Formulation Development Services

From test method development to after-market support, Avomeen’s experienced chemists support all segments of your drug development pipeline. As a full-service CMC/CRO laboratory, we provide customized services that aid pharmaceutical researches, developers, and manufactures.

You’ll be in good hands with our reliance on a Quality by Design (QBD) approach and rejection of the typical list price testing. We recognize that every project is unique, which drives us to spend the time to find out the true nature of our clients’ needs and develop a personalized plan just for you.

Our multi-disciplinary expert scientists and state-of-the-art analytical facilities make us the perfect laboratory to meet your product development needs. Avomeen’s scientists are current with the most sophisticated instrumentation, methods, and technical developments in the industry. Our leading scientists have years of experience with multiple dosage forms, including transdermal delivery systems, ointments, tablets, capsules, films, polymers, coatings, and drug-device combination products.

Why Turn to Avomeen for Your Pharmaceutical Development Needs?

-Direct Consultation with PhD Level Chemist

-Rapid Turnaround on Requests for Proposal (RFP)

-Project Customization (No Cookie Cutter Quotes)

-Wealth of Knowledge & Technical Expertise

-Responsive Staff who are Flexible to Your Needs

-Non-Routine Investigative Problem Solvers – 65% of our Technical Staff are PhD Chemists

-Rush Services Available – We Can Work Within Even the Tightest Deadlines

Services Offered

Pre-Formulation/Formulation Development

-API, Excipient, Impurities, & Drug Product R&D

-Clinical Trial Material Manufacturing (Phase I-IIa)

cGMP Analytical Testing & Development

-Method Development, Validation & Transfer

-Raw Material & Compendial (Pharmacopoeia) Testing
-ICH Stability & Degradation Studies

-Analytical Characterization & Monograph Testing (USP, EP, BP, JP, FCC, ACS, AOAC, AOCS)

-Residual Solvents, Trace Metals, & Heavy Metals

-Q1/Q2 Determination & Deformulation Analysis

-Contaminant & Elemental Impurity Identification

-Dissolution, Elution, & Drug Product Release Profiles

Packaging

-Extractables & Leachables

Litigation Support Services

-Counterfeit Identification

-Patent Infringement

As one of America’s fastest growing independent contract companies, we hope to grow with you as your full-service partner, not just your testing lab. Avomeen is FDA Registered & Inspected, GLP/cGMP Compliant, DEA-Licensed, and ISO 17025-Accredited.

 Contact Us Today for a Complementary Initial Consultation with one of our PhD Chemists