Utilising our experience in the Pharmaceutical Industry we can conduct audits of pharmaceutical development and manufacturing plants, covering cGMP, safety, and OECD GLP.
We have personal experience of auditing laboratories and manufacturing plants in UK, USA, throughout the EU and also in Japan and India. PJC can conduct pre-Regulatory agency audits, couple that with pre-audit training or FDA/EMEA audit awareness training and we can help your business avoid costly delays, oversights or mistakes.
Additional associates can be added to the team to meet clients requirements, such as Pharmaceutical Microbiology, Facility or Process Validation.
We will be happy to discuss your specific requirements.