We are a contract pharmaceutical development organization that helps turn ideas into cures with a complete spectrum of CMC solutions for pharmaceutical development. View more...

Accu-Break Accu-Break Pharmaceuticals, Inc. and Azopharma Product Development Group, Inc. have formed a strategic alliance to provide patented and patent pending tablet technologies and development services to the pharmaceutical industry. For more information click here or visit www.accubreak.com

	Preclinical Services Azopharma provides preclinical metabolism and toxicology services to support your IND filing.
	Synthetic Services Azopharma offers custom synthesis in support of pharmaceutical product development from milligram to kilogram quantities.
	Active Pharmaceutical Ingredients Azopharma has custom synthesis capabilities to manufacture cGMP supplies of active pharmaceutical ingredients.
	Characterization Services From impurity identification to primary reference standards, our synthetic, organic and analytical chemists can assist with routine or challenging characterization projects.
	Large Molecule Capabilities Azopharma provides specialized services specific to the needs of the Biotechnology industry.
	Preformulation Services We specialize in the design and execution of pertinent preformulation activities required for successful pharmaceutical product development.
	Formulation Development Azopharma offers formulations development for dosage forms including Solid Oral, Semi-Solids, Liquids and other non-traditional dosage forms.
	Methods Development & Validation Azopharma's holistic approach to analytical methods development and validation, whether routine or non-routine, ensures compliance with today's industry standards.
	QC and Microbiology Testing Azopharma offers quality control (QC) testing for Active Pharmaceutical Ingredients (API's), pharmaceutical intermediates, excipients, and finished products.
	Stability Studies Core services at Azopharma for management of stability programs are geared towards high throughput production combined with detailed compliance strategies.
	CTM Manufacturing and Packaging Azopharma’s cGMP facilities, experienced team and unique approach to CTM manufacturing give our sponsors an opportunity to accelerate development of their lead compounds.
	Product Development Services- Phase I Express™ Azopharma's proprietary approach for expediting drug development for new compounds entering clinical development activities.
	Contract Manufacturing Azopharma operates manufacturing facilities and provides services to accelerate development, scale-up and commercialization for numerous dosage forms.
	Cytotoxic and Potent Compound Formulation Azopharma has multiple containment suites for developing and manufacturing potent and cytotoxic drug compounds.
	Inhalation Capabilities Azopharma’s inhalation and intranasal formulations development group assists our partners with the development of various inhalation dosage forms.
	Regulatory Consulting We can help navigate the regulatory hurdles associated with drug development and to facilitate approval of submissions by international regulatory authorities.
	Bioanalytical Our GLP compliant operations are equipped to analyze biological samples for drug candidates and metabolites in various biological matrices.
	Drug Delivery Technology Azopharma’s drug development efforts are based on technology platforms including bioavailability enhancement of poorly soluble drugs and the development of customized release profiles.
	Clinical Pharmacology Azopharma’s new state of the art clinical pharmacology research unit brings together an impressive blend of experience and services to support studies across virtually every therapeutic indication.