• 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® IR Service 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.

 

* Indicates a required field 

*1. What is the required release profile? (example – 85% in 15 minutes…)

 

 2. Name of active ingredient (e.g. Ibuprofen) or my drug is similar to _______? (Tablet or Capsule)

*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. Do you require a film coating sample at this time? Specific color?

13. Are there any coating restrictions?

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