The Power of Clinical Trial Supply Management
Bringing new drugs to market presents numerous challenges, but clinical trial supply chain issues can be mitigated by partnering with an experienced clinical trial supply management company. Here at UPM Pharmaceuticals, we specialize in clinical batch manufacturing, packaging, and distribution of oral solid dose pharmaceuticals for both clinical and commercial products. By optimizing your clinical supply chain, UPM ensures the seamless delivery of clinical trial materials, helping to mitigate risks and support the success of your trials.
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Choose a CDMO That Excels at Clinical Trial Supply Management
Selecting the right partner is crucial to the success of your clinical trial. You need a CDMO that offers comprehensive clinical trial supply management, utilizing an appropriate analytical framework and formulation design to ensure optimal production. Look for a partner that provides full-service clinical trial supply chain management, including:
- Clinical trial material planning
- Production forecasting
- Sourcing clinical trial material, including secondary vendors
- Project management
- Clinical data development
Clinical Trial Supply Services from Concept to Commercialization
All-in-one clinical trial supply solutions offer seamless technology transfer of the formulation process and superior manufacturing results. When your clinical batch manufacturing partner manages the entire clinical trial supply chain process, scaling up becomes more efficient, ensuring your product's smooth transition from concept to commercialization. By integrating clinical supply chain management with manufacturing expertise, your CDMO can streamline every step, minimizing risks and maximizing success.
Why Choose UPM as Your Clinical Batch Manufacturing Partner?
UPM is a leading CDMO with extensive expertise in clinical trial supply management, specializing in oral solid dosage and semi-solid manufacturing. We are a family-owned business based in the USA that focuses on cultivating long-term relationships with each of our clinical drug development partners.
Our comprehensive range of clinical trial supply services include formulation and analytical development, quality and regulatory support, seamless technology transfer and scale-up, and more to help you realize your development objectives.
We ensure the quality of drugs produced for clinical trials with our well-controlled manufacturing processes will lead to in-process blend uniformity. Our expert team also manages excipients, API, packaging components, and third-party resources to optimize your clinical supply chain.
At UPM, we specialize in advancing our customers' formulation development efforts through:
- Experience - We have more than 25 years of experience as a trusted CDMO in clinical trial supply chain management.
- Responsive Team - We believe that customizing our partnerships yields the best results, and because of our size, we can respond and adapt with ease.
- Clinical Data Development - You can reduce the time from drug development to marketing thanks to the high-quality, reliable and statistically sound data collected.
- Manufacturing Capacity - Our 475,000 square foot research and production facility provides us with the capability to meet your generic pharmaceutical needs thanks to our annual one-shift production potential of:
- 700 million capsules
- 4 billion tablets
- 1,300,000 kilogram units of semi-solids
- Temperature-Controlled Warehouse - With almost 300,000 square feet of surveilled and mapped storage, we can ensure the stability and security of your product.
- Controlled Substance Capacity - We have 16,000 square feet of DEA-approved vault space available for secure storage of controlled substances.
Frequently Asked Questions Clinical Trial Supply Chain Management
What is clinical trial supply chain management?
Clinical trial supply chain management involves the planning, coordination, and distribution of investigational products to ensure a timely and adequate supply at trial sites. It covers everything from procurement and production to logistics and inventory management.
Why is clinical trial supply management critical in clinical trials?
Effective clinical trial supply management is crucial to ensure that the right investigational products are delivered to the right sites and participants at the right time, preventing delays and protecting the integrity of the trial.
What are the key components of clinical trial supply chain management?
The key components of proper clinical supply management include demand forecasting, procurement, storage, packaging, labeling, distribution, temperature control, inventory management, and accountability for returned or unused supplies.
How does UPM support clinical trial supply logistics?
UPM provides comprehensive clinical trial supply logistics, managing every aspect of the supply chain, from clinical batch manufacturing to distribution, ensuring seamless execution and compliance with regulatory requirements.
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Our Experience & Comprehensive Services Make Us Your Complete Clinical Trial Supply Management Solution
At UPM Pharmaceuticals, we specialize in customized, large-scale pharmaceutical production, providing end-to-end clinical trial supply solutions. From conceptualization and clinical trial supply chain management to product launch, we ensure seamless execution at every stage. To learn more about how our clinical trial supply services can support your clinical batch manufacturing needs, contact us or call (423) 989-8000. Partner with UPM and experience the benefits of working with a clinical trial supply management expert.
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