Solid Formulation
Although solid dose formulations are one of the most established dosage forms in pharmaceuticals, the path to market can still be blocked by critical obstacles such as API stability, release kinetics, and bioavailability limitations.
Our high-quality raw materials and functionalized excipients form a comprehensive portfolio that addresses all your most pressing challenges in solid formulation manufacturing, with products that include:
Solid Formulation Products
Related Product Resources
- Article: Active Pharmaceutical Ingredient (API) Stability in Solid Dose Formulation
This article describes the use of excipients to help address API stability issues.
- Article: API Solubility and Dissolution Enhancement Via Formulation
Our overview of API solubility and dissolution enhancement methods can help you decide between the many options to take during formulation.
- Article: Solid Formulation Development Using Melt-based 3D Printing Technologies
3D printing can overcome challenges during formulation development, with a focus on enhancing API bioavailability in solid dispersions. Find out how in this technical article.
- Article: Improving API Solubility Using Hot Melt Extrusion Formulation With Polyvinyl Alcohol
Find out how Hot Melt Extrusion with polyvinyl alcohol (PVA) is used to enhance API solubility.
- Article: Dry Granulation in Solid Oral Formulation: Advantages of Spray-Dried Mannitol in Roll Compaction
In recent years, mannitol has gained popularity as an excipient in solid dosage formulation due to its beneficial physicochemical properties.
- Article: Use of Mannitol as an Excipient for Solid Drug Formulation
This article describes the advantages of mannitol when used as an excipient in solid drug formulation.
- White Paper: API Stability in Solid Dose Formulation: Exploring the Myth of Inert Excipients
Stable active pharmaceutical ingredients (APIs) represent a critical success factor for drug formulation for four main reasons.
- White Paper: New Opportunities for Oral Sustained Release Formulations with Polyvinyl Alcohol
Achieving the appropriate release kinetics for an active pharmaceutical ingredient (API) is essential to ensure success of the therapeutic.
- White Paper: Considerations for Dosing Accuracy in a New Carrier for Dry Powder Inhalation
Inhalation drug delivery methods are attractive, noninvasive routes when rapid onset of action, minimal side effects and excellent bioavailability are desired.
- Download: Formulation Handbook
Formulating pharmaceutical dosage forms: In this formulation handbook, we have compiled information and formulation examples that can help you when developing your formulation.
Our particle optimized Parteck® functional excipients, for example, are specifically developed to address formulation challenges in solid dose, featuring unique particle properties and outstanding individual functionalities. The result is excellent tableting behavior and simplified formulation design, so you can speed your product to market.
In addition, you can rely on our industry-leading Emprove® Program to meet today’s complex regulatory challenges with a superior combination of comprehensive documentation and transparency. Our high-quality raw materials, regulatory expertise, and dedicated support provide everything you need to simplify supplier qualification, speed up processes, and reduce your total cost of ownership.
RELATED WEBINARS
Continuous Manufacturing in Solid Dose - How to Leverage Opportunities of This New Technology
Coating with Polyvinyl Alcohol: When Coating Runs Smoothly
Hot Melt Extrusion with PVA: A New Opportunity for Shallenging APIs
Solubility Enhancement, Stability and Scalability of Mesoporous Silica Formulations: from Lab to Production Scale
Total Cost of Ownership – How the Choice of Excipients Makes Your Economics
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