• Core Excipients

  • Functional Excipients for the Formulation of Solid Oral Dosage Forms

  • Coatings

  • Fully Formulated Conventional and Modified Release Film Coating Systems
  • Formulation Tools

  • Useful Tools for the Pharmaceutical Formulator

  • Education

  • Technical formulation and development seminars and forums
  • Evaluate

  • Competitor, Consumer Color Preference, Regulatory, Tablet Library of Shapes, and Trademarks

  • Develop

  • Unique Tablet Designs and Branding Solutions

  • Visualize

  • Concept to Prototypes using State-of-the-Art 3D Images and Models through our Tablet Design Centers

  • Brand Security

  • Understand Options and Learn of New Technologies to Protect your Brand
  • Technical

  • Global Technical Support, Technical Service Labs and Tablet Design Centers

  • Regulatory

  • Global Regulatory Support Services

  • Customer

  • Global Customer Support and Service Locations
  • Tools

  • Useful Tools to Assist Pharmaceutical Product Development

  • Literature

  • Extensive Collection of Articles, Product Literature, Application Data and Regulatory Documents

  • Education

  • Technical Formulation and Development Seminars and Forums
 

HyperStart® Formulation Questionnaire

For further information about this service and to receive a free-of-charge formulation recommendation, please fill in the form below.

This service is completely CONFIDENTIAL and none of your details will be shared with any other party.

 

If you already have project details then please complete the following information as fully as possible. We will then propose a formulation to you.

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*1. What is the required release profile? Please give all relevant time points, e.g. 2 hours 10%, 8 hours 60%, 12 hours >80% 

 

 2. Name of active ingredient, e.g. Ibuprofen

* 3. Active dose, e.g. 250mg

*4. Drug Solubility in water (mg/ml or part per parts)

5. Is the solubility pH dependent? If yes, what is the pKa of the drug?

 6. List any unacceptable materials 

* 7. What is your target maximum tablet weight?

8. Target markets, are there any limitations relating to compendial requirements?

*9. What is your preferred manufacturing method: Direct Compression/ Wet Granulation / Roller Compaction?

10. What are your dissolution testing conditions: dissolution media, USP I, II or III, agitation speed, use of sinkers, etc.?

11. Any other information?, e.g. drug sensitivity (light/heat/moisture), micronized API, melting temperature, etc.

12. Would you like to arrange a technical trial at a Colorcon laboratory?

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