Freyr label 360 is a Pharmaceutical Labeling Software that Supports End to End Label Management, Label Tracking and Deviation Management for...
Freyr provides Regulatory Software Solutions to support Global Lifesciences companies that include Pharmaceuticals, Medical devices, Cosmetics and...
Freyr Reports provide Regulatory Intelligence, Market Intelligence; Trend Analysis Reports which include information on global/regional Regulatory...
Freyr iREADY is a technology based Cosmetic Ingredient Database platform and it provides Regulatory compliance support to manufacturers for...
Freyr provides End to End Chemical Regulatory Compliance services to health care consumers like product registration, notification, Formulation...
Freyr provides end to end regulatory support for Food/dietary supplements manufacturers in product registration/notification and classification...
Freyr provides end to end Cosmetic Regulatory Services like formulation; ingredient review, label review, claims review, safety assessment;...
Freyr provides Chemical Safety Consulting service to chemical and consumer companies in product hazard identification and risk assessment....
Freyr offers complete scientific report writing, Data Scouting, Regulatory Intelligence and Strategy services for different consumer products with...
Freyr provides end to end chemical Regulatory services to cosmetics and biocides in the product Notification and Registration as per the...
Freyr helps in Scientific Report Writing, development of Product data sheets (PDS), preparation of position papers, REACH registration and...
Freyr provides regulatory support in Supply chain regulatory compliance, Formulation review, Raw material compliance and Document management...
Freyr provides regulatory intelligence services for medical device manufacturers to meet region-specific health authority requirements for...
Freyr provides medical device regulatory compliance, gap analysis and remediation services for medical device manufacturers that span across UDI,...
Freyr provides labeling and promotional material regulations support for medical devices manufacturers, which include label creation and review of...
Freyr provides end-to-end medical device labeling services for medical device manufacturers that span across label creation, review of IFU (...
Freyr provides regulatory support for medical device manufacturers in device technical file publishing, which include creation, review, validation...
Freyr provides regulatory support for medical device manufacturers in preparation of Design History File (DHF) document, which include Design Plan...
Freyr provides ISO 14971 Risk Management consulting services for medical device manufacturers that span across the preparation of comprehensive...
Freyr helps In-Vitro Diagnostic Device (IVD) manufacturers in Performance Evaluation Report (PER) preparation, development of Performance...
Freyr provides Post Marketing Surveillance (PMS) support for medical device manufacturers, which includes development of Post-market Surveillance(...
Freyr provides regulatory support for medical device manufacturers in preparation of Clinical Evaluation Report (CER), which includes report...
Freyr SUBMIT Pro is one of the best eCTD software tool which helps Life science companies in various regulatory submissions to global health...
Freyr SUBMIT Pro is an prominent eCTD publishing Software with various features like Inbuilt eCTD validator and viewer, submission tracking, HA...
Freyr SUBMIT Pro is one of the best eCTD Submission software that suits all kinds of Regulatory eCTD publishing and submission requirements across...
Freyr SUBMIT Pro is an cloud hosted, on-premise cost effective eCTD submission software with features like eCTD Submission tracker, Viewer,...
Freyr provides medical device regulatory services in LATAM that span across medical device registration/notification, local representation support...
Freyr provides medical device regulatory services in RoW Market that span across medical device registration, notification and local...
Freyr provides end-to-end regulatory services for medical devices manufacturers in Europe to comply with the new EU MDR regulations for successful...
