Pharmaceutical Consultancy,  Let Us be Your Quality Subject Matter Expert

We have the great expertise to provide a comprehensive range of current best practices across all GxP sectors. With over the last 13 years of success in designing, implementing, reviewing and continuously improving pharmaceutical quality system (QMS) and compliance in the pharmaceutical manufacturing sector.  We possess the excellent practical knowledge to keep our clients compliant with the current best practices and regulatory requirements. With projects ranging from the most basic to the very complex we can tailor our services to you to provide the right level of support for your business needs.  

We can help you in reduction of deviations significantly through implementing excellence in deviation management process, finding out the potential root cause and effective CAPA implementation process. Also, we can support you in creating a culture of quality, maintaining quality standards, compliance and continuous improvements throughout the manufacturing operations.

We have great experience in auditing pharmaceutical quality system, GMP facilities.  We can conduct mock audits to assess best practices and identify issues that could affect the quality of manufactured pharmaceuticals and become compliance issues with EU GMP V4/MHRA, FDA, ISO 9001, WHO. Our experts are qualified lead auditors.

We have experience excellence in GxP Data Integrity which is critical to Patient Safety, Regulatory Compliance and Business Success. Make our Data Integrity Services an essential part of your organization’s journey toward a sustainable, compliant and successful company-wide data governance and integrity program.