CEO en oprichter van GCP Central, Marieke Meulemans, spreekt regelmatig in Europa bij industri\u00eble evenementen, belangenorganisaties, universiteiten, non profit instellingen en zakelijke bedrijven.<\/p>\n
Marieke Meulemans heeft GCP Central<\/a> in 2012 opgericht en is de drijvende kracht achter de duidelijke visie die het bedrijf heeft. Zij heeft gezondheidswetenschappen gestudeerd en heeft meer dan 15 jaar ervaring in de life science industrie. Doordat ze heeft gewerkt voor de top 50 bedrijven in de farmaceutische industrie, CROs en trainingen heeft gemaakt voor klinisch onderzoek voor academische ziekenhuizen, heeft ze goede kennis van regelgeving opgebouwd. Deze kennis combineert zij met haar ervaring met strategisch leermanagement en innovatieve online leermethodes. De missie van Marieke is om GCP-kennis een belangrijk onderdeel te maken van de dagelijkse praktijk en de kwaliteit van onderzoek te verbeteren. Ze wil de achterhaalde jaarlijkse GCP training vervangen door een vooruitstrevende continue leermethodiek in de life sciences industrie.<\/p>\n Haar passie om GCP training toegankelijk te maken voor druk belaste professionals en haar wens om die eindeloze powerpoints in benauwde trainingslokalen achter zich te laten, maakt haar een boeiende en bevlogen spreker. Marieke’s unieke presentatiestijl en enthousiasme en expertise in klinisch onderzoek zullen flair geven aan uw volgende conferentie of webinar.<\/p>\n Taal:\u00a0 Nederlands, Engels<\/p>\n Marieke’s discussies hebben betrekking op verschillende onderwerpen, waaronder:\u00a0<\/span>\u00a0<\/span><\/p>\n<\/li>\n Hoe je GCP kennis tastbaar kan maken voor je (site) medewerkers<\/em><\/p>\n<\/li>\n [\/et_pb_text][et_pb_button button_url=”https:\/\/gcpcentral.com\/nl\/contact\/” button_text=”WIL JE ONS UITNODIGEN ALS SPREKER OP JE EVENEMENT?” button_alignment=”left” admin_label=”Spreker button” _builder_version=”4.27.6″ custom_button=”on” button_text_size=”22px” button_text_color=”#414146″ button_bg_color=”#f3ea41″ button_border_width=”18px” button_border_color=”#f3ea41″ button_border_radius=”0px” button_font=”|600|||||||” button_use_icon=”off” custom_padding=”|30px||30px” hover_enabled=”0″ custom_css_main_element=”text-transform: uppercase;||” locked=”off” global_colors_info=”{}” sticky_enabled=”0″] [\/et_pb_text][et_pb_text _builder_version=”4.16″ global_colors_info=”{}”]<\/p>\n <\/a><\/p>\n <\/em><\/span><\/p>\n<\/li>\n <\/em>Clinical Trials Arena, January 27, 2022. Article by Reynald Casta\u00f1eda and William Newton <\/em><\/p>\n <\/em><\/p>\n<\/li>\n <\/em><\/span><\/p>\n<\/li>\n <\/p>\n<\/li>\n <\/em><\/span><\/p>\n<\/li>\n <\/em> <\/span><\/p>\n <\/em><\/span><\/p>\n<\/li>\n <\/em><\/span><\/li>\n <\/em><\/span><\/p>\n <\/em><\/span><\/p>\n<\/li>\n <\/em><\/span><\/p>\n <\/em><\/span><\/p>\n<\/li>\n <\/em><\/span><\/p>\n <\/em><\/span><\/p>\n<\/li>\n Marieke and co-panelists discussed the upcoming changes to regulations and clinical trials, and the key points to remember during this lively panel<\/em>.<\/span><\/p>\n <\/span><\/p>\n<\/li>\n In this webinar, Marieke spoke of how to drive better quality clinical research through continuous learning, and how this can save time and money, and reduce the risk of non-compliance.<\/em><\/span><\/p>\n <\/span><\/em><\/span><\/p>\n<\/li>\n <\/em><\/span><\/p>\n <\/em><\/span><\/p>\n<\/li>\n <\/em><\/span><\/p>\n <\/em><\/span><\/p>\n<\/li>\n <\/em><\/span><\/p>\n <\/em><\/span><\/p>\n<\/li>\n GCP Central hosted a webinar for EUCROF \u201cHow To Navigate Your Clinical Trials In The Time Of Corona\u201d. In this article, (Dutch language), it discusses Marieke\u2019s \u00a0development of learning sessions for the EUCROF Events & Training Working Group.<\/em><\/span><\/p>\n <\/em><\/span><\/p>\n<\/li>\n Continuous learning is the way of the future. Explore how your company can respond faster and more flexibly to industry changes with host Marieke Meulemans of GCP Central.<\/em><\/span><\/p>\n <\/em><\/span><\/p>\n<\/li>\n
\n[\/et_pb_button][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_image src=”https:\/\/gcpcentral.com\/wp-content\/uploads\/2022\/04\/marieke-meulemans-press-and-speaking-gcp-central-scaled.jpg” alt=”marieke meulemans press and speaking gcp central” title_text=”marieke meulemans press and speaking gcp central” align=”center” align_tablet=”center” align_phone=”” align_last_edited=”on|desktop” _builder_version=”4.16″ background_color=”#f7ea21″ mix_blend_mode=”overlay” global_colors_info=”{}”]
\n[\/et_pb_image][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ _builder_version=”4.16″ background_color=”#EFEFEF” global_colors_info=”{}”][et_pb_row _builder_version=”4.16″ width=”75%” max_width=”75%” use_custom_width=”on” width_unit=”off” custom_width_percent=”75%” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_text _builder_version=”4.16″ text_font=”|||on|||||” header_font=”||||||||” header_2_font=”|800|||||||” header_2_text_color=”#414146″ header_2_font_size=”34px” header_2_line_height=”1.1em” locked=”off” global_colors_info=”{}”]<\/p>\nIN DE PERS<\/h2>\n
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Oracle Podcast, March 28, 2022. Hosted by Katherine Vandebelt, with Sebastian Payne of Deloitte\u00a0<\/span>
Marieke Meulemans discusses with an expert panel how the implementation of streamlined regulatory processes will benefit patient health and clinical research in the European Union.
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Xtalks Webinar, January 27, 2022.\u00a0 Co-panelists: Pierre Omnes (Syneos Health), Paulien Nuyts (Deloitte), Leona Fitzgerald (ACRO), Sylvia Mareki (EMD Serano), Elvin Thalund (Oracle Health Services).<\/span>
A discussion panel on the EU 536\/2014 regulation and the essential changes that businesses must make to avoid delays in clinical trials. <\/em> <\/span>\n
<\/span>Marieke was interviewed by Clinical Trials Arena over the implementation of EUCTR, and the impact of CTIS on clinical trials.<\/em><\/span><\/p>\n
<\/em>Forschungsdock, 21 November and 16 December, 2021<\/span>
Marieke presented on the essentials to be ready for the implementation of CTIS and EU CTR. <\/em><\/span>\n
Dutch Clinical Research Foundation (DRCF) Online, December 15, 2021<\/span>
In this Dutch language interview, Marieke Meulemans was interviewed to share her experiences with the European Clinical Trial Regulation (EU CTR) and the associated Clinical Trial Information System (CTIS).
<\/em><\/span>\n
VFENR – Dagvoorzitter(Chairman), November 25, 2021<\/span>
Chair for the symposium. <\/em> <\/span>\n
<\/span>Podcast for EUCROF Events & Training Working Group. \u00a019 November 2021 \u00a0Guest speaker: Sebastian Payne of Deloitte.\u00a0 <\/span>
In this podcast, Marieke is joined by Sebastian Payne of Deloitte to discuss the questions raised during the recent \u201cEMA Clinical Trials Information System (CTIS) \u2013 Be Ready Before It Goes Live\u201d webinar and the benefits for clinical research organisations.\n
<\/em>ACRON\/DCRF 11 November, 2021 November, 2021 – Chairman\/Dagvoorzitter\u00a0<\/span>
Interviewer\/Chair for the symposium.\n\n
In this Dutch language article, Marieke discusses the importance of organizations being prepared for both VGO and the introduction of the CTIS portal in the EUCTR. <\/em> <\/span>\n
ACRON and VIG, 24 August and 16 September, 2021.\u00a0<\/span>
Marieke Meulemans (GCP Central and also reviewer of the EMA CTIS training courses) shows which training programs are currently available, where they can be found and supports the preparation of CTIS with useful tips and practical information. <\/em> <\/span>\n
<\/em><\/em>EUCROF Webinar, April 26th, 2021<\/span>
Marieke navigates those involved in clinical trials through the new EMA training program, and where to find relevant training materials, and helps with preparing teams on how to use CTIS.<\/em> <\/span>\n
<\/em>Panelist at the EU Site Solutions Summit<\/a>, April 21, 2021. Co-Panelists:\u00a0 Rianne Tooten and Isabelle van der Haegen. Facilitator: Vivienne van der Walle.<\/span> <\/span>\n
<\/em>Webinar for the <\/span>United Conference of Clinical Trials and Clinical Research<\/a>, April 15, 2021<\/span> <\/span>\n
United Conference on Drug Development and Industrial Pharmacy, Live Webinar April 7, 2021<\/span>
In this live webinar, Marieke shared compliance and education tips for the GMP & GLP workforce. <\/em> <\/span>\n
EUCROF, 16 September 2020<\/span>
Marieke presented the challenges and learning moments of GCP Central as they went through the validation process for myGCP with EUCROF in this engaging webinar. <\/em> <\/span>\n
Presenter, May 2020<\/span>
Validation of software tools in the conduct of clinical trials is a requirement described in the ICH-GCP guideline, applicable to drug research globally, and implemented in local legislation, including the EU legal framework and the US Code of Federal Regulations (CFR). Marieke Meulemans guides you through the experiences of GCP Central as they completed the validation process for myGCP. <\/em> <\/span>\n
<\/span>ACRON website, 2 June, 2020 <\/span>Article by ACRON <\/span>\n
<\/em>GCP Central Webinar, November 2019. <\/span>\n
Dutch Clinical Research Foundation, 26 & 27 June, 2019.\u00a0<\/span>
Annelies van Woudenberg (DCRF) and Marieke Meulemans (GCP Central) presented the first training offered by the DCRF Academy: the e-learning about ECTR, the new European legislation for setting up and conducting clinical research with medicines<\/em>.
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