On October 12 and 13 Sophidis Days will take place in Tunis, Tunisia. This conference is one of the events of the year in the North African pharmaceutical market and RC REDOL will be there, on the 12th, RC REDOL’s Technical Director, Eng. Ana Gonçalves, will lecture at the Sophidis Days conference on various topics related to Good Manufacturing Practices.
In preparation for the event, we have published articles, here, about some of the topics that will be addressed, vital issues for pharmaceutical production, which will be further developed in the conference. However, we have left out a significant number of issues that will also be covered at the conference. We are talking about points such as procedures for Out of Specification situations, Qualification of Suppliers, Qualification of Equipment, Systems, and Facilities, Comparison of current and future legislation for the production of sterile products “Eudralex Volume 4 Annex 1” or the Analytical Validation, Validation of IT Systems and Risk Management.
Together with the topics presented in past publications, all these points are also vital to succeed in EU and FDA audits. Therefore, if you need to know how to obtain a certification process, have good results in audits and get market approval for the production or distribution of a pharmaceutical product, do not hesitate in contacting RC REDOL.
Our technical team, led by Ana Gonçalves, is a specialist in Good Manufacturing Practices and has a large experience in the Pharmaceutical Industry, essential conditions for an efficient consulting for your processes. Visit us on Sophidis Days and don’t miss an opportunity to access the best of the European pharmaceutical market, in Maghreb.
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