Blog Alberto Carazo Sin categoría 0 comentarios 13 - 01 - 15
1.Introduction The EMA has approved on the 20th of November 2014, the new guide “Guideline on setting health based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities”. Once approved, this guide will have to […]
Read moreBlog Miguel Ruiz Biosafety, Clean rooms, Pharmaceutical support, Sin categoría 0 comentarios 11 - 12 - 14
INGELYT, through our partner QUALIA, has attended the last CHINA PHARM 2014
19th edition of CHINA-PHARM, hold in Shenzen the last October, the fair occupied more than 30.000m2 with 431 exhibitors from 22 countries.
In cooperation with QUALIA , INGELYT introduced some of its high specialized products, as the airtight doors with pneumatic seal.
In addition INGELYT introduced the new services of consultancy and advising focused to the Pharmaceutical Industry.
Blog Juan Carlos Carballo Sin categoría 0 comentarios 17 - 09 - 14
1. INTRODUCTION For some time at public and private research centers and national and international production centers specifically designed facilities are being used for containment of dangerous biological agents in its manipulation and that could be a risk for the […]
Read moreBlog Alberto Carazo Sin categoría 0 comentarios 10 - 09 - 14
1. Introduction: Primary packaging suppliers are reporting investments in order to increase the use of primary materials pre-sterilized, “Ready to Use” (RU). These materials open up new possibilities and opportunities in the design of sterile manufacturing areas. 2. What’s […]
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