{"id":841,"date":"2026-03-25T15:12:59","date_gmt":"2026-03-25T14:12:59","guid":{"rendered":"https:\/\/viqi-group.com\/?page_id=841"},"modified":"2026-10-09T16:51:38","modified_gmt":"2026-10-09T14:51:38","slug":"domaines","status":"publish","type":"page","link":"https:\/\/viqi-group.com\/en\/domaines\/","title":{"rendered":"Areas"},"content":{"rendered":"\t\t
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SP\u00c9CIALISTE DES LIFE SCIENCES<\/span><\/h1>\t\t\t\t<\/div>\n\t\t
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Chez VIQI, nous accompagnons les acteurs des Life Sciences sur l\u2019ensemble des m\u00e9tiers cl\u00e9s du secteur.<\/p>

Pharmaceutique, dispositifs m\u00e9dicaux, biotechnologies : nous intervenons sur les domaines strat\u00e9giques et techniques, de la R&D \u00e0 la mise sur le march\u00e9, pour soutenir vos projets.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

\n\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\tPrendre rendez-vous avec un expert<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Nos domaines
\nd\u2019expertise<\/span><\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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R&D Pharmaceutique<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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D\u00c9VELOPPEMENT DE PRODUITS PHARMACEUTIQUES, DE LA MOL\u00c9CULE AUX LOTS CLINIQUES<\/strong><\/p>

Screening formulation et d\u00e9veloppement gal\u00e9nique<\/p>

D\u00e9veloppement analytique<\/p>

D\u00e9veloppement et tests de conditionnement primaire et secondaire<\/p>

\u00c9tudes de stabilit\u00e9 (ICH)<\/p>

Analyses de risques qualit\u00e9, proc\u00e9d\u00e9s<\/p>

Interaction contenant\/contenu<\/p>

\u00c9tudes de pr\u00e9-formulation et caract\u00e9risation API \/ excipients<\/p>

Lancement des lots de d\u00e9veloppement et pilotes<\/p>

Pr\u00e9paration de la documentation CMC et dossiers de d\u00e9veloppement<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t

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R&D DISPOSITIFS M\u00c9DICAUX<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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DISPOSITIFS M\u00c9CANIQUES, \u00c9LECTRO M\u00c9DICAUX, IMPLANTABLES, COMBIN\u00c9S, ET IVD<\/strong><\/p>

Conception, prototypage et faisabilit\u00e9<\/p>

Analyses de risques selon ISO 14971<\/p>

Biocompatibilit\u00e9 selon ISO 10993<\/p>

Usability Engineering selon IEC 62366<\/p>

Documentation DHF compl\u00e8te<\/p>

D\u00e9finition et pilotage du plan de v\u00e9rification et validation (V&V)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t

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R&D LOGICIEL<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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D\u00e9veloppement logiciel pour dispositifs m\u00e9dicaux et syst\u00e8mes industriels<\/strong><\/p>

D\u00e9finition de l’architecture syst\u00e8me<\/p>

Gestion des exigences et sp\u00e9cifications<\/p>

D\u00e9veloppement, tests unitaires, int\u00e9gration<\/p>

Validation logicielle selon IEC 62304<\/p>

Cybers\u00e9curit\u00e9 selon IEC 81001-5-1<\/p>

Compatibilit\u00e9 avec l’\u00e9lectrom\u00e9dical (IEC 60601) lorsque applicable<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t

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ING\u00c9NIERIE & INDUSTRIALISATION<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Industrialisation des proc\u00e9d\u00e9s pharmaceutiques et dispositifs m\u00e9dicaux<\/strong><\/p>

Transposition industrielle et scale-up<\/p>

Travaux neufs et cr\u00e9ation de zones GMP<\/p>

Transferts de production site \u00e0 site<\/p>

URS \/ CDC \/ FS \/ DS et analyses de risques<\/p>

FAT \/ SAT et coordination fournisseurs<\/p>

Suivi de chantier, installation, revamping et qualification initiale<\/p>

Am\u00e9lioration continue<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t

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Qualification, validation & CSV<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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CONFORMIT\u00c9 DES \u00c9QUIPEMENTS, PROC\u00c9D\u00c9S ET SYST\u00c8MES
<\/strong><\/p>

Strat\u00e9gie de qualification \/ validation et analyses de risques<\/p>

Qualification des \u00e9quipements, utilit\u00e9s et infrastructures (FAT \/ SAT \/ QI \/ QO \/ QP)<\/p>

Validation des proc\u00e9d\u00e9s de fabrication, nettoyage et st\u00e9rilisation<\/p>

Qualification des \u00e9quipements de laboratoire et syst\u00e8mes analytiques<\/p>

Validation des syst\u00e8mes informatis\u00e9s : ERP, MES, LIMS, GED, SCADA\u2026<\/p>

Conformit\u00e9 GAMP 5 \/ 21 CFR Part 11 \/ Annexe 11<\/p>

Maintien de l\u2019\u00e9tat qualifi\u00e9 et valid\u00e9 tout au long du cycle de vie<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t

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AUTOMATION & IT INDUSTRIELLE<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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DIGITALISATION, PILOTAGE ET PERFORMANCE DES SYST\u00c8MES INDUSTRIELS
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Architecture des syst\u00e8mes automatis\u00e9s et infrastructures industrielles<\/p>

Programmation et configuration des automates, IHM et syst\u00e8mes SCADA<\/p>

D\u00e9veloppement et optimisation des s\u00e9quences, recettes, interlocks et alarmes<\/p>

Int\u00e9gration des syst\u00e8mes OT \/ IT et interfaces \u00e9quipements<\/p>

Supervision, historisation et gestion des donn\u00e9es industrielles<\/p>

D\u00e9ploiement et \u00e9volution des syst\u00e8mes MES et outils de production<\/p>

Diagnostic, fiabilisation et am\u00e9lioration des syst\u00e8mes automatis\u00e9s<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t

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LABORATOIRE DE CONTR\u00d4LE<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Laboratoire de contr\u00f4le<\/strong><\/p>

D\u00e9veloppement et validation de m\u00e9thodes<\/p>

Gestion des OOS, OOT et investigations analytiques<\/p>

Application stricte des principes ALCOA<\/p>

Support aux transferts de m\u00e9thodes<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t

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ASSURANCE QUALIT\u00c9 & DATA INTEGRITY<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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SYST\u00c8MES QUALIT\u00c9, CONFORMIT\u00c9 ET MA\u00ceTRISE DES DONN\u00c9ES
<\/strong><\/p>

Gestion des d\u00e9viations, NC, CAPA et Change Control<\/p>

Investigations qualit\u00e9 et r\u00e9solution des probl\u00e9matiques complexes<\/p>

Pr\u00e9paration et accompagnement des audits et inspections<\/p>

Mise en place, optimisation et digitalisation des QMS<\/p>

Gouvernance des donn\u00e9es et conformit\u00e9 Data Integrity (ALCOA+)<\/p>

Accompagnement des op\u00e9rations en environnement GMP<\/p>

D\u00e9ploiement des SI Qualit\u00e9 : eQMS, GED, LIMS, ERP\u2026<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\t\t\t

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AFFAIRES R\u00c9GLEMENTAIRES<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Conformit\u00e9 r\u00e9glementaire sur tout le cycle de vie des produits<\/strong><\/p>

DM : Dossiers de marquage CE et 510(k)<\/p>

Pharma : Cr\u00e9ation et mise \u00e0 jour des dossiers d’AMM<\/p>

Soumissions r\u00e9glementaires : Enregistrements internationaux (US, EU, ROW)<\/p>

Transition MDR et maintien de conformit\u00e9<\/p>

PMS : Pharmacovigilance et Mat\u00e9riovigilance<\/p>

R\u00e9ponses aux autorit\u00e9s de sant\u00e9<\/p>

\u00c9valuation clinique (CEP\/CER)<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t

\n\t\t\t\t<\/stop><\/stop><\/radialGradient><\/defs><\/rect><\/rect><\/g><\/path><\/g><\/svg>\t\t\t<\/div>\n\t\t\t
\n\t\t\t\t<\/stop><\/stop><\/radialGradient><\/defs><\/rect><\/rect><\/g><\/path><\/g><\/svg>\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Les ATOUTS de
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Des expertises d\u00e9di\u00e9es \u00e0 chaque domaine cl\u00e9 <\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Une capacit\u00e9 de r\u00e9ponse rapide et agile <\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Un haut niveau d\u2019exigence en mati\u00e8re de conformit\u00e9<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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Une approche guid\u00e9e par le sens du service<\/h3>\t\t\t\t<\/div>\n\t\t\t\t
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QUELQUES CLIENTS DE LA <\/span>PHARMACEUTIQUE<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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QUELQUES CLIENTS DU <\/span>DISPOSITIF M\u00c9DICAL<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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<\/div>\n\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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VIQI, votre partenaire de confiance dans le secteur des Life sciences<\/span><\/h2>\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\t\t\t\t\t\t\n\t\t\t\t\t\t\n\t\t\t\t\t\t\t\t\tD\u00e9couvrir Notre histoire<\/span>\n\t\t\t\t\t<\/span>\n\t\t\t\t\t<\/a>\n\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"

SP\u00c9CIALISTE DES LIFE SCIENCES Chez VIQI, nous accompagnons les acteurs des Life Sciences sur l\u2019ensemble des m\u00e9tiers cl\u00e9s du secteur. Pharmaceutique, dispositifs m\u00e9dicaux, biotechnologies : nous intervenons sur les domaines strat\u00e9giques et techniques, de la R&D \u00e0 la mise sur le march\u00e9, pour soutenir vos projets. Prendre rendez-vous avec un expert Nos domaines d\u2019expertise R&D […]<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":0,"menu_order":10,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-841","page","type-page","status-publish","hentry"],"yoast_head":"\nNos domaines d'expertise Life Sciences | VIQI<\/title>\n<meta name=\"description\" content=\"VIQI accompagne les acteurs des Life Sciences sur tous les m\u00e9tiers cl\u00e9s : R&D pharma, dispositifs m\u00e9dicaux, ing\u00e9nierie, qualit\u00e9, validation et r\u00e9glementaire.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/viqi-group.com\/en\/domaines\/\" \/>\n<meta property=\"og:locale\" content=\"en_GB\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Nos domaines d'expertise Life Sciences | 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