{"id":37,"date":"2013-10-09T13:21:07","date_gmt":"2013-10-09T11:21:07","guid":{"rendered":"http:\/\/localhost\/wordpress\/index.php\/consultants-registry\/"},"modified":"2026-08-10T18:06:28","modified_gmt":"2026-08-10T16:06:28","slug":"consultants","status":"publish","type":"page","link":"https:\/\/www.darqa.org\/index.php\/language\/en\/consultants\/","title":{"rendered":"Consultants"},"content":{"rendered":"\n\n
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Consultants<\/h1>\n \n\n \n

This directory lists consultants and companies affiliated with DARQA. They offer their expertise and commercial support to DARQA members and third parties. Please contact them directly for more information.<\/p>\n \n\n \n

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Expertise<\/th>\n Company<\/th>\n Services<\/th>\n Name<\/th>\n Phone<\/th>\n Contact<\/th>\n Website \/ profile<\/th>\n <\/tr>\n <\/thead>\n
GCP \u2013 ICH (human), GCP \u2013 VICH (veterinary), GLP (preclinical, laboratory, veterinary and field studies), GMP<\/td>\n ChrisalisQAdvice<\/td>\n Auditing, consultancy, training and quality-system support<\/td>\n Christine Mitchell<\/td>\n +31 6 11 52 92 56<\/a><\/td>\n Christine.mitchell@chrisalisqadvice.com<\/a><\/td>\n chrisalisqadvice.com<\/a><\/td>\n <\/tr>\n
GMP, medical devices and ISO<\/td>\n Progress \u2013 Experts in Life Sciences<\/td>\n Auditing, consultancy, training, quality systems, processes, document management, validation and project management<\/td>\n Edwin van den Bos<\/td>\n +31 (0)23 563 5016<\/a><\/td>\n sales@progress-lifesciences.nl<\/a><\/td>\n progress-lifesciences.nl<\/a><\/td>\n <\/tr>\n
GMP, GCP, GLP, GCLP, medical devices and ISO 17025<\/td>\n QUALITY & RISK MANAGEMENT zw-frl<\/td>\n Auditing, consultancy, training, quality systems, risk management, CAPA, validation and inspection support<\/td>\n Karin Baas<\/td>\n +31 6 51210120<\/a><\/td>\n karin.baas@mac.com<\/a><\/td>\n qa-rm.com<\/a><\/td>\n <\/tr>\n
GLP field studies<\/td>\n Marie-Antoinette Smit QA Services<\/td>\n Consultancy, auditing and training<\/td>\n Marie-Antoinette Smit<\/td>\n +31 6 40436390<\/a><\/td>\n Marie-AntoinetteSmit@masqas.nl<\/a><\/td>\n Professional profile<\/a><\/td>\n <\/tr>\n
GMP and Regulatory Affairs (IMPD\/eCTD)<\/td>\n Pharma Max Consult<\/td>\n Quality assurance, auditing, training, computerised-system validation, project management, due diligence, quality-system design and regulatory dossier support<\/td>\n Maxim Mikhalevitch<\/td>\n +31 6 53232712<\/a><\/td>\n info@pharmamax.nl<\/a><\/td>\n pharmamax.nl<\/a><\/td>\n <\/tr>\n
GMP, GLP, GDP and GCLP<\/td>\n Forest Pharma Consultancy<\/td>\n Quality-assurance support, QP\/RP services, audits, regulatory-document review, CMC and quality systems<\/td>\n Wen Liem<\/td>\n +31 (0)6 31 95 12 32<\/a><\/td>\n wliem@forestpharma.nl<\/a><\/td>\n forestpharma.nl<\/a><\/td>\n <\/tr>\n <\/tbody>\n <\/table><\/figure>\n \n\n \n

Contact details were checked against the consultants\u2019 own websites or current professional profiles on 10 August 2026. Where no current first-party website was available, this is noted below.<\/p>\n \n\n \n

For Marie-Antoinette Smit QA Services, the telephone number and email address come from DARQA\u2019s January 2026 registration. Her current professional profile confirms her QA\/GLP background, but the contact details could not be independently confirmed.<\/p>\n \n\n <\/div>\n \n\n \n

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