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Clinical Evaluation Report, CER, Medical Device Regulation, Europe

Core Label management software, Label Tracking | Freyr LABEL 360

Cosmetic claims substantiation, Cosmetic Claims review, Therapeutic claims

Cosmetic Ingredient Database, Cosmetic Formulation Software

Cosmetic ingredient review, Cosmetic ingredient analysis

Cosmetic labeling Requirements, Cosmetic labeling Review

Cosmetic Packaging, Cosmetic Packaging and Labeling, Artwork

Cosmetic Product Information File, PIF Compilation, PIF Cosmetics

Cosmetic Product Registration South Korea, MFDS

Cosmetic regulatory affairs, Cosmetic regulatory compliance

Cosmetics Classification, Cosmetic Registration, Notification, EMA, USFDA

Cosmetics labeling requirements, US, Europe, China, Australia, India, Korea

Cosmetics Market Strategy, Product Registration, Licensing, Notification

Cosmetics Regulatory Services, Cosmetic Regulations, Freyr

Design history file, DHF remediation, DHF, Medical devices, USFDA

Device Technical File Publishing, Device technical file, DTF, Medical devices

Dossier Template, CTD template, CTD dossier, USFDA, EU

eCTD publishing Software, eCTD format, eCTD validator

eCTD Software cost, Request a Demo, eSubmission Software

eCTD Submission, eCTD publishing requirement

eCTD submissions for better Health Authority Compliance

EMA Released Brexit related guidance for pharmaceutical companies

EMA’s guidance on GMP and GDP flexibilities during Covid-19

EMA’s revised guidelines on the quality of water for pharmaceutical use

EU - Cosmetics Claims Compliance

EU Cosmetic Claims, Annex III - Free From, Annex IV - Hypoallergenic, cosmetic products

EU MDR and its Impact on Medical Device Labeling and Artwork

EU MDR Compliance of Medical Devices – Exclusive Webinar

EU MDR Compliance, EU MDR regulations, European Medical Device Regulation

EU MDR new Corrigendum for Class I Medical Devices

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