Contract Drug Development
Services
UPM is both a contract development organization and a contract manufacturing organization as our services range from early stage development services to GMP manufacturing services.
We’ve designed our company around the three main attributes
Contract Pharma says clients look for in a CRO.*
1) Fast and responsive service.
2) Personal involvement.
The scientist assigned to you is your project leader.
3) Our invoices tie directly to your milestone deliverables.
Our commitment to these attributes enable us to deliver industry-savvy, customer-focused services.
Scientific Expertise – Access to some of the industry’s best analytical chemists, formulation design specialists, and manufacturing specialists who are known for developing innovative solutions to difficult development challenges.
Technologies – UPM’s proprietary technologies can be utilized in our clients’ product line extension programs, such as reformulation of drugs to sustained release, fast-disintegrating tablets or pediatric formulations.
Rapid and Responsive Turnaround Our scientists and managers utilize daily planning meetings and a master scheduling process that provides for timely and responsive project management.
Quality Assurance Documentation and Regulatory Support – Our highly experienced quality assurance and regulatory personnel implement complete cGMP quality and regulatory systems that support formulation development, clinical batch manufacturing, and analytical work-up.
* Canavan N. Formulation development opportunities abound. Contract Pharma, October 2006.
