IPEC Europe and APV are delighted to invite you to our 11th annual conference on pharmaceutical excipients.
We are looking forward to welcoming you in Rotterdam, The Netherlands.
The conference will be held on two days: from Wednesday (morning) until Thursday (evening) and will focus on regulatory topics relating to pharmaceutical excipients and technology.
The day one will focus on regulatory topics and we will offer five presentations and three “workshops”. We will open the conference with a presentation in IPEC Federation followed by a talk on Supply chain security and the related IPEC Federation position paper. The remaining of the presentations will cover current hot topics like recent FDA requirements for excipients supplier and the EMA Q&A on co-processed excipients.
The regulatory workshops aim to provide detailed practical information about current topics supporting industry to comply with regulatory requirements and other expectation. These “workshops” will be held two times in parallel to allow participants to attend two of the three sessions. These sessions will allow practical exercises and discussions related to the topics covered. Participants will have the opportunity to exchanges their personal experience with colleagues out of the same industrial and regulatory environment.
Since excipients are key parts of the formulation of medicines, we will open the second day with a talk from USP on Novel Excipients followed by a presentation on “how will the FDA PRIME program support the development of new excipients“. Afterwards we will take the opportunity to listen to a variety of subjects such as impacts of excipients on oral bioavailability, coated tablet performance, and the use of 3D printing for an efficient tablets production, an automated and DoE based development of oral solid dosage forms as well as the use of a complete line of excipients for hard-shell capsules.
