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Freyrsolutions

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Freyr provides biocidal/disinfectant product classification and regulatory services as per the country specific regulations across the globe.
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Freyr helps in Scientific Report Writing, development of Product data sheets (PDS), preparation of position papers, REACH registration and consultation services for consumer product compliance.
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Freyr offers complete scientific report writing, Data Scouting, Regulatory Intelligence and Strategy services for different consumer products with global regulations.
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Freyr provides End to End Chemical Safety Regulatory Affairs (CSRA) services to consumer products manufacturers in product registration, classification, toxicology assessment, safety data sheet development and regulatory intelligence services as per region specific regulatory requirements for market approvals.
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Freyr provides End to End Chemical Regulatory Compliance services to health care consumers like product registration, notification, Formulation review and We offer EU REACH and CLP Registration/Dossier Update, Hazard Communication for quick market access.
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Freyr offers legal representative services to food supplement manufacturers in product registration, post-marketing and serve as a liaison between manufacturer and HA in taking up all applicable regional responsibilities.
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Freyr provides scientific and regulatory support to Nutraceuticals/ Food/ Dietary supplements manufacturing companies for food claims review services across the globe.
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Contact Freyr for Global End-to-end Food Supplement regulatory services to comply with Health Authority Requirements.
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Freyr provides End to end regulatory support for food supplements manufacturers which include registration, classification and process clearances to comply with region-specific regulatory requirements for successful market entry of products across the globe.
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Freyr provides end to end regulatory support for Food/dietary supplements manufacturers in product registration/notification and classification across the globe.
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Freyr provides Cosmetics Regulatory Intelligence/Information services for product classification, registration, claims, labeling & Packaging requirements, local agent requirements and regulation across globe
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Freyr provides end-to-end cosmetic safety services which include cosmetic safety assessment, preparing cosmetics safety assessment reports (CPSR), toxicological risk assessment and toxicological reports.
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Freyr provides compliant cosmetic claims review with Cosmetic Claim Substantiation, literature reviews and marketing claims to comply with regional health authorities
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Freyr provides end to end Cosmetic Regulatory consultation support, starting from Regulatory intelligence to responsible person services for cosmetics and personal care companies across the globe.
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Freyr provides end to end Cosmetic Regulatory Services like formulation, ingredient review, Cosmetic Labeling, Cosmetic Claims, safety assessment, toxicology services, dossier compilation and market entry support.
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Freyr provides Swiss Authorized Representative(CH-REP) services for medical device manufacturers outside the Switzerland as per Swissmedic regulations.
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Freyr provides United Kingdom Responsible Person(UKRP) services for medical device manufacturers outside the UK as per MHRA regulations.
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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.
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Freyr provides Swiss Authorized Representative(CH-REP) services for foreign medical device manufacturers and acts as Swiss distributor/importer of devices across Switzerland.
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Freyr provides Swiss Authorized Representative(CH-REP) services for medical devices and IVD manufacturers in CE marking and labeling support as per Swissmedic regulations.