Welcome to DARQA!
The Association aims to serve as a platform for developments regarding quality, quality systems, and quality policy within organizations and institutions operating in the fields of medical and pharmaceutical science, in the broadest sense of the term.
It seeks to achieve this objective by, among other things:
a. Exchanging information and insights regarding current quality systems, GxP-relevant guidelines and directives from government bodies (including the EMA and MHRA), and ISO standards;
b. Monitoring, promoting, and—where possible—influencing developments in this field;
c. Enhancing the expertise of members in the areas of quality and quality policy;
d. Maintaining and fostering contacts with individuals and institutions within government and other organizations whose activities intersect with DARDA’s field of work.
Events
News
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Verslag vervolgprogramma ALV 11 april 2025 ‘Kwaliteit binnen en tussen de GxP’s’
Details: Verslag vervolgprogramma ALV 11 april 2025 ‘Kwaliteit binnen en tussen de GxP’s’We denken dat we dezelfde taal spreken op het gebied van Quality Assurance (QA). Maar wist je dat een ‘Principal Investigator’ in GLP iets heel anders betekent dan in GCP? Wist je…
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Newly released OECD Position Paper on Good Laboratory Practice and IT Security
Details: Newly released OECD Position Paper on Good Laboratory Practice and IT SecurityThis week the OECD published the OECD Position Paper on Good Laboratory Practice and IT Security (No 25) Data generated according to Good Laboratory Practice (GLP) are increasingly generated and retained in…
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Summary of ICT theme day on audit trails (review) and data integrity, 31 May 2023
Details: Summary of ICT theme day on audit trails (review) and data integrity, 31 May 2023On Wednesday 31 May 2023 DARQA hosted a theme day addressing the practicalities of audit trails and audit trail reviews in pharmaceutical and medical information management systems. The session was based on…
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Verslag DARQA themadag over ”process mapping”, 8 april 2022
Details: Verslag DARQA themadag over ”process mapping”, 8 april 2022Na de webinars van de afgelopen tijd was deze themadag over “process mapping” op 8 april 2022 in Amersfoort, na de ALV, een goede gelegenheid om weer eens in workshopverband te werken.…
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Latest news on OECD Chemical Safety
Details: Latest news on OECD Chemical SafetyNew reports on good laboratory practice The principles of Good Laboratory Practice (GLP) are applied in the performance of tests to obtain data on the properties and hazards for people, animals and…
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Key elements of the OECD Framework for MAD and GLP
Details: Key elements of the OECD Framework for MAD and GLPThis video recording provides an overview of the OECD’s Mutual Acceptance of Data (MAD) framework as well as the OECD Principles of Good Laboratory Practice. The framework ensures the quality…
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DARQA webinar Post-Authorization (Safety) (PASS) Studies, 8 oktober 2021
Details: DARQA webinar Post-Authorization (Safety) (PASS) Studies, 8 oktober 2021Op vrijdag 8 oktober jl. vond een webinar plaats met als onderwerp “PASS”. Beide presentaties werden gegeven in het engels. The first presenter is Stuart Harris, Astellas. Stuart explains to us why…
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DARQA webinar GCP audits and inspections experiences
Details: DARQA webinar GCP audits and inspections experiencesOp vrijdag 18 juni jl. vond een webinar plaats met als onderwerp “GCP audits and inspections experiences during COVID-19 clinical studies”. Beide presentaties werden gegeven in het engels. The first presenter…