Freyrsolutions

Freyr provides end to end regulatory artwork services & solutions for Food Supplements companies which include artwork management, artwork design & pack management, artwork studio and proofreading services

Freyr provides end to end regulatory artwork services & solutions for Medical device companies which include artwork management, artwork design & pack management, artwork studio and proofreading services

Freyr provides end to end regulatory artwork services for Pharmaceutical companies which include artwork lifecycle management, artwork design & pack management, artwork studio and proofreading services.

Freyr & team is specialized in creation of label content, tracking technical change specifications, creating artworks, managing artwork launch requests, integrating Regulatory text changes etc

Freyr provides artwork regulatory affairs labeling services for life science companies and supports global & regional/local labeling management.

Freyr offers Artwork Proofreading Services to Pharma, Biotech, food supplements and cosmetic companies by our proofing experts to achieve the artwork towards right-first-time (RFT) approval

Freyr offer unique Artwork graphic design services which include logo creation, identity design and brand promotion as per regulatory guidelines for the Life Science Companies.

Freyr provides Artwork Coordination services for new product launch, amendments to existing designs/products, promotional designs, Artwork submission, PLD - Private Label Division, print vendor logistics, packaging

For Pharma Artwork staffing and artwork lifecycle management, Freyr has qualified Artwork Management professionals suiting to clients' onsite engagements which include Artwork Consultant, Artwork Designer, Artwork Proofreader/QC, Regulatory Affairs Associate for Labeling and Artwork etc

Freyr provides packaging artwork management consulting services for pharma, biotech, medical device, cosmetics and food supplement companies.

Freyr provides Product lifecycle management (PLM) tool to create comprehensive processes and workflows for end-to-end packaging artwork lifecycle management.

Freyr provides Global Regulatory Artwork Management Services & Solutions for life sciences Industry, which include Artwork proofreading, Artwork packaging, Artwork Lifecycle management, Artwork Studio Services.

Freyr helps medical device manufacturers with language translation, editing of medical device technical information in IFU, DSURs, SUSARs, Package inserts & labels for submission & approval process as per targeted regional languages with compliance to ISO 17100:2015 & ISO 9001:2008 standards.

Freyr provides Staff Augmentation Consulting services for medical device manufacturers that span across several Regulatory functionalities from associate to expert level resources and 24X7 time zone coverage model to support multiple time zone and office coverage.

Freyr provides regulatory supports for medical devices and In-vitro diagnostics (IVD) manufacturers in registration, regulatory submissions, dossier compilation, GAP analysis, premarket notification, local agent services and classification as per country-specific regulatory requirements for compliant market entry.

Freyr provides regulatory strategy consulting services for medical device manufacturers looking for global expansion in complex markets like APAC, MENA & LATAM and supports in device registration, classification, assistance with notified body selection and regulatory submissions.

Freyr provides regulatory support to the medical device manufacturers in De-Novo registration of medical devices in the USA that span across classification, Pre-Submission/Q-Submission meeting request, risk benefit determination, De-Novo submission package compilation, publishing and creation for Pre-Submissions.

Freyr provides regulatory intelligence services for medical device manufacturers to meet region-specific health authority requirements for compliant market entry of their products and provides comprehensive regulatory Intelligence reports corresponding to organizational needs basing on the region and device type.

Freyr provides medical device regulatory compliance, gap analysis and remediation services for medical device manufacturers that span across UDI, GDPR, EUDAMED compliance support, post approval compliance support, Consultation and representation services for ISO 13485:2016, MDSAP, BGMP and establishment of QMS document

Freyr provides labeling and promotional material regulations support for medical devices manufacturers, which include creation & review of IFU (Instructions for Use), UDI compliance, GAP analysis, comprehensive artwork check, tracking and maintaining label changes.