A Full Service CDMO with End-to-End Capabilities

Adare Pharma Solutions provides flexible services for contract development and manufacturing, including clinical trial materials, product development, commercial manufacturing, and packaging.

As a one-stop CDMO, Adare is capable of developing and manufacturing oral dose products from beginning to end, as well as taking pre-established projects and tech transfer into our facilities.

Commercial Manufacturing Capabilities

Adare provides expertise and regulatory adherence for scale-up and manufacturing of schedules II-IV drug products. Our facilities are fully licensed and inspected by the Food and Drug Administration (FDA) and Drug Enforcement Agency (DEA).

Adare’s team-oriented leadership is made up of results-oriented problem solvers. Our production teams have significant tenure in site operations, and our account teams are made up of regulatory compliance experts who are focused on providing excellent customer service and support.

Our experienced Project Managers are here to guide you through every step of the way and focus on your needs, ensuring that your project is delivered on time. With a detailed-oriented lens, they oversee all the activities and progress of your project.

A Proven Track Record

Adare has provided commercial scale supply of over 40 pharmaceutical brands to more than 100 countries on behalf of blue-chip pharmaceutical companies across the globe.

Adare Pharma Solutions has helped in launching prescription and OTC products for adult and pediatric patient populations, as well as veterinary products. We are experts in coacervation, and we are pioneers in the development of novel drug-delivery technologies.

Lean/Six-Sigma

All sites are trained in Lean/Six-Sigma processes which speed decision making and efficiency. Our manufacturing teams have a collective supply chain mindset to support pre- & post-launch activities. And Adare has the ability leverage co-located drug development resources for the continuity of your drug supply.

Speak With An Expert

Profile Photo: Audrey Butler

Audrey Butler

Senior Vice President, North America Operations

Audrey Butler brings over 25 years of Quality experience to her position as Senior Vice President, Global Operational Excellence. During her career, she’s held positions of increasing responsibility in pharmaceutical manufacturing, including leadership of Analytical Development (R&D), Quality Assurance, Operations, Quality Control, and Project Management.

Audrey has served in the Quality divisions of pharma companies such as Hikma Pharmaceuticals, West-Ward Pharmaceuticals, Boehringer Ingelheim, and Ben Venue Laboratories, Inc

She has a BS in Chemistry from University of Mary Washington and a Masters in Chemistry from University of Maryland.

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