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Formulation Development

At UPM Pharmaceuticals, scientific sophistication and experience come together with flexibility, responsiveness and innovation. UPM provides pharmaceutical drug development services including formulation development, GMP manufacturing, analytical methods development and stability testing.

Our drug development services are characterized by a core commitment to meeting the client's objectives with the highest quality while maintaining the most efficient use of time and controlling costs. Our pharmaceutical development team applies its extensive experience in developing creative solutions to your unique challenges. UPM takes enormous pride in supporting pharmaceutical companies at every step of the of the drug development process.

Throughout the project, we work to advance and optimize your product through scientific and customized approaches. UPM has highly trained staff, detailed scheduling processes, and a broad array of research and manufacturing scale equipment, to ensure your project is successfully completed with quality and on time.

UPM Pharmaceuticals, Inc. provides the following pharmaceutical development support:

  • Formulation development
  • cGMP manufacturing
  • Tableting/Film coating/Capsule filling
  • Fluid bed technology
  • Granulation/Milling/Roller compaction Stability Testing
  • Scale-up and technology transfer
  • Blinding of clinical supplies
  • Pilot to small scale commercial
  • Analytical services
  • Regulatory support DEA licensed/scheduled substances

To find out more details about any of the above offering feel free to stop by and visit our main facility located in Baltimore, Maryland. Also please do not hesitate to contact us with any additional questions at (410) 843-3738.

Formulation Evaluation
  • Content uniformity evaluation
  • Dissolution testing
  • Stability assessment
Regulatory Support
  • SUPAC application support
  • GMP/FDA/ICH guidance
  • Product development strategies
Analytical Services
  • HPLC based
  • Full ICH stability conditions
  • Dissolution testing
Clinical Manufacturing
  • cGMP manufacturing
  • Direct API fill into capsules
  • Dosage form preparation and blinding




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