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 DARQA Themadag 20 april 2018
Details: Verslag DARQA Themadag 20 april 2018“GDPR (General Data Protection Regulation) – AVG (Algemene Verordening Gegevensbescherming)” Locatie: Regardz Berghotel, Amersfoort. Opening Reneé van Boxtel, lid van de GCP-commissie, opent deze dag waar ca. 65 personen aan hebben deelgenomen.…
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Safety Information from a GCP Perspective
Details: Safety Information from a GCP PerspectiveOn Friday, 22 September 2017, a GCP/GPV training day was held with the subject: “Safety Information from a GCP Perspective“. The day started with a presentation on “Core concepts in pharmacovigilance…
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Verslag DARQA Themadag 21 april 2017
Details: Verslag DARQA Themadag 21 april 2017“ICT in het GXP-domein” Locatie: Regardz De Eenhoorn, Amersfoort. Opening Hans de Raad, voorzitter ICT commissie, opent als dagvoorzitter deze themadag “ICT in het GXP-domein”. Er zal vanuit ICT, GCP, GLP en…
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OECD – Environment, Health & Safety News – March 2017
Details: OECD – Environment, Health & Safety News – March 2017GLP Guidance documents An Advisory Document on Test Itemsis being developed by a drafting group, originally under the leadershipof Canada, and now by the United Kingdom, Denmark (Pharmaceuticals) and Italy. The objective…
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No 18: The Relationship between the OECD Principles of GLP and ISO/IEC 17025
Details: No 18: The Relationship between the OECD Principles of GLP and ISO/IEC 17025Op 2 Sep 2016 is er een nieuwe Position Paper van de OECD SERIES ON PRINCIPLES OF GOOD LABORATORY PRACTICE AND COMPLIANCE MONITORING uitgekomen: Regarding the Relationship between the OECD Principles of…
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No 17: Application of GLP Principles to Computerised Systems
Details: No 17: Application of GLP Principles to Computerised SystemsOp 22 April 2016 is een nieuwe Advisory Document of the Working Group on Good Laboratory Practice uitgekomen: Application of GLP Principles to Computerised Systems ENV/JM/MONO(2016)13 dit document vervangt Consensus Document No.…