Blog

STEQ and MERCK promote seminar focused on Sterility

[vc_row full_width=”stretch_row_content_no_spaces” css=”.vc_custom_1564670180706{padding-top: 300px !important;padding-bottom: 220px !important;background: #a3a3a3 url(http://br306.teste.website/~ferra863/steq/wp-content/uploads/2019/08/Img-16.png?id=1266) !important;}”][vc_column][vc_column_text]

STEQ and MERCK promote seminar focused on sterility

[/vc_column_text][vc_separator color=”sandy_brown” border_width=”3″ el_width=”10″][/vc_column][/vc_row][vc_row css=”.vc_custom_1564073259210{margin-top: 25px !important;margin-bottom: 25px !important;}”][vc_column width=”3/4″][vc_column_text css=”.vc_custom_1564671080812{padding-bottom: 20px !important;}”]

STEQ and MERCK promote Seminar Excellence in Waste Processes

On the 15th and 16th of May, the Seminar Excellence in Sterile Processes took place at the Holiday Inn hotel. The event was attended by international speaker David Barbault, technical director of Getinge La Calhène and specialist for the entire line of DPTE Insulators and transfer solutions, in addition to speakers Ana Cadore, Angela Mattos, Silvia Yuko Eguchi and Vitor Oliveira, who addressed topics of extreme relevance. The seminar that took place on the first day of the event, had as its main theme the Innovations and Trends for Microbiological Quality Control, addressing the validated technologies for the execution of aseptic processes, clean rooms x isolators: main differences, applicable standards and directives, qualification and validation of Insulators: methods and procedures, sterility test – A differentiated view and the challenges in Environmental Monitoring of classified areas.

[/vc_column_text][vc_masonry_media_grid grid_id=”vc_gid:1564671067443-fe732af0-6000-3″ include=”1269,1268,1270″][vc_row_inner][vc_column_inner][vc_column_text css=”.vc_custom_1564671091657{padding-top: 20px !important;padding-bottom: 20px !important;}”]On the 16th, the seminar focused on Good Practices in Aseptic Drug Production, where lectures were given on the topics Qualification and Validation of Insulators: methods and procedures, single use for final filling in Insulators, GMP raw materials for the formulation of biopharmaceuticals and pharmaceutical products, validated technologies for the execution of aseptic processes and clean rooms x Insulators. The event was a success and was attended by important customers and experts in the field, interested in improving their techniques and knowledge in the area of sterility. Check out some of the testimonials from the participants: “I thought it was very good, I didn’t know so deeply about insulators and managed to open my mind.”Excellent – Content of the presentation according to the proposed theme and useful information for living in isolators.”

“Very experienced speakers, having optimally clarified all questions.”[/vc_column_text][/vc_column_inner][/vc_row_inner][/vc_column][vc_column width=”1/4″][vc_basic_grid post_type=”post” max_items=”3″ element_width=”12″ gap=”15″ item=”958″ grid_id=”vc_gid:1564671067445-b58ff26f-8e44-9″ taxonomies=”4, 1, 5, 3″][/vc_column][/vc_row]

Artigos Relacionados

Stay up to date with the news!

Receive our updates