We offer formulation development through a highly skilled scientific team with expertise in variety of dosage forms. At our state-of-the-art facilities, we handle simple and complex oral solid dosage forms which include tablets, capsules, powder for suspension and multi-particulate drug delivery systems customized for immediate release, modified release and targeted release.
We provide ‘Fit-for-Purpose’ formulation development to support early phase/ ‘First-in-Human’ studies and also provide end-to-end services up to commercial manufacturing. We also support for development of customized formulations for veterinary use and nutraceutical applications.
Our expert team is having experience in developing complex formulations and provide tailored solutions to your problems and help to optimize the development time and costs.

We offer extensive end-to-end services of formulation development for a wide variety of oral dosage forms. Our team assists from Prototype formulation screening studies, Formulation/process optimization using QBD principles, ICH compliant Stability studies, Scale-up/technology transfer, formulation development to development of First-in-Human (FIH) formulations to enable clinical trial studies from phase I to phase III/ commercial manufacture. We are equipped with state-of-the-art facilities to manufacture 500 to 50,000 units at R&D and up to 7,500,000 units at commercial manufacturing sites and complete CMC support for regulatory submission.

Immediate Release, Delayed Release, Sustained Release, Oral Disintegrating, Film coated, Taste masking, Fixed Dose Combinations (FDC).
a. Single Layer Tablets
Depending on the mode of usage conventional uncoated or film coated immediate release tablets, orally disintegrating tablets, sublingual tablets, buccal tablets, taste masked tablets, effervescent tablets and chewable tablets can be developed
b. Delayed release/ modified release tablets
Proven expertise in formulation of acid labile drugs using delayed release technology and where necessary the drug release can be modulated or targeted to release at specific regions of the gastro-intestinal tract.
c. Bilayer Tablets
A combination of immediate release (loading dose) and modified release portions of a single drug can be incorporated in a single dosage form. Also, a combination of two or more drugs which may be incompatible can be formulated based on the requirement
d. Mini Tablets Fixed dose combination (FDC) or standalone drug molecules can be formulated as minitablets whi>ch offer the advantage of being multi-unit particulate systems
(MUPS) like avoiding dose dumping, tailored drug release profile, targeted to release at specific regions of the gastro-intestinal tract etc.
a. Hard Gelatin Capsules
Powders, pellets, mini tablets or their combination can be filled into hard gelatin capsules
b. Soft Gelatin Capsules
Soft gelatin capsules can be developed for liquids or suspension filling for poorly soluble and thermolabile, photosensitive medicaments.
We develop age appropriate, easily reconstitutable powders for oral suspensions which can be filled into sachets
Services across the product lifecycle
US FDA inspected lab and manufacturing facilities
Experience with advanced formulation technologies
20+ years of experience in formulation
We understand that clear communication is essential to successful collaborations, and that's why we have a dedicated team that is always ready to help you. Whether you have questions about our services, want to discuss a potential partnership, or simply want to learn more about our company, we're here to help.
Our team of experts is dedicated to providing personalised solutions tailored to your unique needs. So, please don't hesitate to reach out to us. We look forward to hearing from you and helping you achieve your business goals.
Aurigene Pharmaceutical Services is a leader in the synthesis of activated MethoxyPolyethyleneGlycol(m-PEGs), With a comprehensive product range and customized services. ...
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October 24th-26th, 2023 | Barcelona, Spain
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