We offer facility and product audits to cGMP standards, based upon our experience of manufacturing and development activities for a range of dosage forms.
PJC Pharma Consulting Ltd provides auditing to cGLP requirements and cGCP worldwide. With extensive experience of hosting regulatory agency audits, we are the ideal partner to assist you in preparation for regulatory agency audits (MHRA, FDA etc).
We use our manufacturing and development experience to help your products progress to market quicker with a ‘right first time’ approach. This approach includes the latest QbD ideas and meets the expectations of ICH Q8 and Q9 from plan initiation of draft plans, to conception, to market.
PJC Pharma Consulting Ltd’s expert consultants work with you to seamlessly expand your existing team, offer extra expertise to resolve your problems, as well as maximise your return on investment.