ANNEX I – FACILITY DESIGN & EQUIPMENT CONSIDERATION

YOU ARE INVITED TO THE ‘ANNEX I – FACILITY DESIGN & EQUIPMENT CONSIDERATION’ SEMINAR

Annex I, as an essential component of Good Manufacturing Practices, sets forth the guidelines for the manufacture of sterile medicinal products. This framework is critical in ensuring the safety, quality, and efficacy of pharmaceutical products that are vital for patient well-being. However, navigating the complexities of Annex I can often be a challenging task in the production process. Rieckermann and ISPE Malaysia organize a joint seminar on discussing the key elements of Annex I, including facility design, equipment consideration and its implications for pharmaceutical manufacturing. Our panel of industry experts will share their insights, experiences, and practical knowledge, offering you valuable guidance on how to implement Annex I requirements effectively into your production process.

Rieckermann and ISPE Malaysia cordially invite you to join us on June 20, 2023 at Le Meridien, Petaling Jaya for this one-day seminar to gain valuable insights, engage in discussions and explore solutions that will help to navigate the intricacies of Annex I