Pharma Pro provides consulting and training services in the following areas:
Manufacturing:We aim at helping our clients add more value with fewer resources. Reducing over production, decreasing wait times / downtime, inventory management, streamlining and optimizing processes and reducing defects is at the heart of what we do. Total Productive Maintenance (TPM), cause and effect diagrams, ERP systems, Flexible Manufacturing Systems (FMS), ABC Inventory Analysis, Benchmarking and Bottleneck Analysis are some of the tools that we use. We use Corrective and Preventive Action (CAPA) and Process Mapping as a tool to detect,break down and simplify the complex work flow associated with the manufacturing process. This allows us to better design/redesign processes to achieve a lean and reliable manufacturing cycle. Our expertise covers the following areas:
Supply Chain:Pharma Pro helps you build an efficient supply chain that revolves around building flexibility, responsiveness and reliability. Our services include:
Regulatory ServicesRegulatory expectations and industry standards continue to evolve globally. In conjunction with our partners, we offer a wide range of Quality and Regulatory Compliance Services. Our services include:
Quality ServicesOur services include: |. Quality Assurance. ||. Quality Control. UP
Feasibility ServicesWe provide complete analysis to assess the economic feasibility of setting up pharmaceutical projects. We cover:.
Documentation SystemsAs per GMP "if it is not written down, then it did not happen". Documents provide information on when, where, who, why and how to complete a task. Documents provide evidence proving that the tasks have been completed as they should be. In a GMP environment, documentation needs to meet certain requirement to ensure product quality and product safety. If an instruction or record is poorly documented, then the manufacture or quality assurance/control of a product can be negatively impacted, potentially reducing patient safety.
Pharma Pro gives helps the companies meet industry standards by following Good Documentation Practices. Pharma Pro enables the companies to outline the expected GDP standards, particularly those unique to each company needed to provide background history, preserve knowledge and learning, protect intellectual property, provide legally valid evidence and ensure the quality and consistency of processes/ activities/manufacturing.UP