Pharma Solutions

Your Problem-Solving Partner

Part of Ingredion Incorporated (NYSE: INGR), a global innovative ingredient solutions provider, we partner with formulators seeking functional materials to enhance formulation performance and overcome their technical challenges.

Our solutions include binders, fillers, superdisintegrants, lubricants, gelatin replacers for softgel, emulsions for encapsulation, viscosifiers, and parenteral APIs.

We combine GMP Facilities, Regulatory Assistance, Global presence, and collaborative Technical Support to be Your formulation Problem-Solving Partner.

Our values


Our values

We are committed on delivering solutions to formulation challenges, with relevant technical
and regulatory support globally.

Consumer Preferred Solutions
We develop and invest in materials that provide relevant functionality and high value to formulators that enable
delivery of consumer-preferred products.

Compliance & Support
Through a dedicated team, we provide Global
Regulatory assistance and Collaborative technical

Reliable Supply
We have over 50 years of legacy supplying parenteral grade anhydrous dextrose, high function specialty starches, pharma
grade mannitol, and other polyols to pharmaceutical formulators globally.  We are now adding other specialty excipients, all manufactured under cGMPs.

Meet your partners

Pharma team

Regulatory & Quality

We are committed to provide you a
Global Regulatory Assistance,
no matter where you operate

Quality Assurance

Providing cGMP mannufacturing and EIP documentation

We manufacture our excipients using the highest quality raw materials and in adherence to cGMP standards published by
IPEC (International Pharmaceutical Excipients Council) in the Good Manufacturing Guide.  We actively participate in IPEC
to contribute to the strengthening of standards that assure patient safety and efficacy.  Our plant quality teams monitor
our products through rigorous in-process testing and conduct annual product reviews to ensure we are in compliance with
and meet USP-NF, Ph. Eur. , JP and IP requirements.

Our regulatory team is staffed with pharmaceutical industry-trained experts.  They have built a full range of documents
customers require to assist with product registration globally, including in China.  You can find a summary of the regulatory
documentation available for each product in the respective EIP Index (Excipient Information Package Index).  That contains
a list of the documents available.  Those marked as Basic in the EIP Index are available to download from the website.  The
documents marked as On Demand can be accessed via written request to

Technical Services

Learn more about our Collaborative Technical Support

Technical Services

Our central laboratory in Bridgewater, NJ, USA is well equipped with experts in processing and applications to bring fundamental understanding of structure function relationships. In 2024 we will open new applications laboratory in Ahmedabad, India, staffed by experienced formulators. In addition, our business partners bring their own laboratories to support our customers globally. We seek to provide customers with relevant technical information to enable them to solve their formulation challenges quickly.

Contact us

Are you looking for information about our
solutions or seeking support?

Let's talk