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PHARMACEUTICAL DEVELOPMENT AND CLINICAL TRIAL MATERIALS

YOUR COMPOUND IN THE CLINIC. QUICKLY. COST-EFFECTIVELY. END OF STORY.
Why choose Metrics for the development and manufacture of your critical compounds? The answer is easy, once you know the Metrics difference.

THE METRICS DIFFERENCE
• A pharmaceutical development staff with an average of 16 years' career experience
•Advanced scientific expertise from PhDs, Master and Registered Pharmacists and Chemists
• Flexible, state-of-the-art manufacturing facility and equipment
• Potent and toxic drug handling capabilities
• DEA-registered for Schedule II-V

• A pharmaceutical development staff with an average of 16 years' career experience
• cGMP Facility with excellent FDA track record
• Analytical support from over 80 chemists

AND WHAT IT MEANS FOR YOU
• You’ll receive experienced and timely recommendations and decision-making regarding:
      • insoluble actives
      • unstable actives
      • potent and toxic actives
      • small molecule delivery
      • large molecule delivery (oral dosage only)
• Fast-track development from NCE to first-in-man in 4 to 6 months
• Expedited ANDA submission to FDA in 12 to 15 months
• Scale-up services and seamless technical transfers
• Batch sizes of less that 1 kg up to 400 kg
• One-on-one, direct communication with project scientists
• Fast-track development for Phase I-III

Clinical Trial Materials (Phase I - III)

  • tablets
  • capsules
  • bead-filled capsules (nonpareil and extruded)
  • overencapsulation
  • liquid-filled hard gels, for Phase I
  • creams, ointments, liquids for Phase I

Final Formulation Expertise in:

  • immediate release
  • sustained release
    • matrix tablets/capsules
    • coated tablets
    • coated beads
  • fast dissolve
  • chewable tablets
  • soft gels
  • extrusion and spheronization


Ready to learn more? Click here to request more information, or to be contacted about your specific needs.

Pharmaceutical Development
Clinical Trial Materials


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