Quality Processes Tailored to Meet Your Phase-Specific Needs
Throughout the product lifecycle, manufacturers face challenges with multiple obligations and demands. From patient safety and quality assurance to cost and schedule requirements, there is a lot that can go wrong. To decrease risk, you need an effective process optimization approach in place, one that streamlines your procedures while increasing the likelihood of product success.
ProPharma Group’s process optimization methodology tailors the approach to help you overcome any challenges and translate your risk tolerance into actions that meet regulatory expectations. Our experts help optimize your manufacturing processes at any point in the product lifecycle — from instilling confidence in your Phase I Clinical supplies to resolving issues that may be threatening the continuity of your commercial supply.
Increased Value Throughout the Product Lifecycle
ProPharma Group’s process optimization methodology is superior because it is:
- Risk-based – Identification, ranking, control, and consensus
- Data-driven – Leverage, wise generation, and clear conclusion
- Comprehensive – Lifecycle, systems, and expertise
- Customizable – Targeted, scalable, and complementary to existing process
Our team applies our extensive process improvement knowledge to fine-tune resources and maximize value creation. Our resources and depth of experience enable us to enhance your capacity and capabilities. We support your evolving regulatory, risk, cost, and schedule constraints, aligning to provide synergies with other processes:
- Clinical Supply
- CMC Development
- Technology Transfer
- Validation and Continuous Process Verification