The topics of the agenda were chosen in close cooperation and with the support of the Iranian FDA.
The goal of this conference is to provide attendees with a thorough overview on new regulations and new developments in manufacturing technology especially for Parenterals.
The conference starts with a plenary session on the Pharmaceutical Landscape in Iran with the general director of the IFDA, Prof. Dinarvand, speaking about the Regulatory Perspective and Framework.
In eight sessions, a broad range of manufacturing aspects will be presented, covering primary packaging components and devices, Blow-Fill-Seal Technology and isolators, fill-finishing operations and freeze-drying, final product testing, labelling and secondary packaging, logistics and good distribution practices. The presentations will address new technologies but also include the latest regulatory and pharmacopoeial requirements.
The conference program has been designed to initiate and support discussion and professional exchange through carefully selected scientific presentations that we believe will foster a vivid interaction amongst all participants. Hear directly from experts in the field on key issues such as Process Concepts, Equipment and Machine Technology, Components, New Methods and Regulatory Trends. This conference aims to provide a platform to foster a dialogue among the various entities committed to pharmaceutical development, manufacturing, testing and quality assurance.
Following PDA’s principles, it is our global aim to provide attendees with sound scientific content as well as the opportunity for discussion and exchange. There is a vendor exhibition, exposing attendees to state-of-the-art machinery and equipment,
as well as service providers – all this will surely offer you an excellent opportunity for learning about new developments, keeping yourself up-to-date with current trends and get the opportunity to engage with industry leaders, getting connected and, last but not least, realizing new business opportunities.