GMP Services

CiPharma provide GMP compliance and quality consulting services, training, auditing and sourcing solutions for the life sciences industry. Our consulting services include PIC/s, FDA and EMA GMP compliance advice that is based on cost-effective and practical compliance approaches suited to work with and meet your business demands.

Whether your organization needs experienced GMP professionals to complete key tasks or a large long term project our consultants have a wide range of GMP skills and knowledge that will help your achieve your goals.

If you have an impending audit  or have just been audited, our auditors can determine if you are ready, need to make improvements or formulate your response to the regulator’s audit or compliance report. Our audit service’s also extend to providing third party GMP assessments to verify your suppliers, in line with “best practice” for the pharmaceutical sector.

CiPharma’s project management services help you get production running and comply with the relevant regulations. We offer a full range of validation services, from cleaning validation and process validation to computer systems validation as well as consultancy on registration strategies and submissions for companies wishing to enter new markets.

We are also experts in implementing and upgrading Quality Management Systems (QMS) for life sciences clients. Also learn how we apply the processes used in other industries, such as Lean Manufacturing and Six Sigma within the regulatory constrains of the Pharmaceutical industry.