Since its formation in 2000, PCS has established relationships with clients across a variety of sectors within the healthcare industry, supporting projects in Pharmaceutical, Over the Counter, Consumer Goods and Nutritional products.
Headed up by a statistician with over 20 years industry experience, PCS is able to work on long-term projects or offer support on an ad hoc basis, dependant on the particular needs of the client.
Whether your piece of research is for a full regulatory submission, or simply for internal decision making, we always adhere to the principles of ICH GCP. We appreciate the importance of the regulatory framework that clinical research operates under, and always work to the standards of the appropriate regulatory agency, whether it's FDA or EMA for Pharmaceutical and OTC products, or the European Food Safety Authority for Nutritionals. Keeping abreast of the latest industry statistical standards and guidance ensures the results we deliver are robust and will meet the highest level of scrutiny.
Expert statistical input into the protocol to ensure your study is appropriately designed to answer the objectives.
Development of a suite of SAS programs to generate report ready tables, figures and data listings.
Utilisation of historical data and relevant publications to provide sample size estimates.
Preparation of a statistical analysis plan, and usage of the most appropriate statistical methods to leverage your study data.
Preparation of randomisation schedules.
Statistical input into the clinical study report and analyses for publications.