Freyrsolutions.in receives about 4360 visitors in one month. That could possibly earn $21.8 each month or $0.73 each day. Server of the website is located in the United States. It took our server 3.09 seconds to reach and load the main page of Freyrsolutions.in. This does not include JavaScript, image and CSS files load timing. This is a good result. This result is good enough, but there is a room for improvement. If you would like to investigate please refer to the link at the bottom of this page.
Traffic and Value
| Is freyrsolutions.in legit? | |
| Website Value | $393 |
| Alexa Rank | 1077138 |
| Monthly Visits | 4360 |
| Daily Visits | 146 |
| Monthly Earnings | $21.8 |
| Daily Earnings | $0.73 |
Freyrsolutions.in Server Location
Country: United States
Metropolitan Area: Scottsdale
Postal Reference Code: 85260
Latitude: 33.6013
Longitude: -111.8867
Summarized Content
Freyrsolutions Main Page Content
| HTML Tag | Content | Informative? |
|---|---|---|
| Title: | Global Regulatory Solutions and Services | Could be improved |
| Description: | Freyr is a Global Regulatory Solutions and Services company, focusing on the entire Regulatory value-chain ranging from Regulatory Strategy, Intelligence, Dossiers, Submissions to post approval maintenance, Labeling, Artwork Change Management for Pharmaceutical, Generics, Medical Device, |  |
| H1: | A Leading, Global, Regulatory Solutions & Services Company | |
| H2: | Pharmaceuticals Expertise | Is it informative enough? |
| H3: | Cost-EffectivePaper to eCTD Conversions For Global Formats | |
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• Title contains 48 characters. We think that you could improve this tag by adding more relevant information or keywords.
• Take a look at the headings; there might be too little information. Headings are important for usability and search engine optimization.
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Internal Pages
| /regulatory-affairs-services: | |
|---|---|
| Title |
Global Regulatory Affairs, CMC Regulatory Affairs Services, Pharma |
| Description |
Freyr provides Global Regulatory affairs services to Consumer, Pharma & Bio - Pharma companies with product development, registration and commercialization, new product and market authorizations, Health Authority submissions, post approvals, CMC Regulatory Affairs and lifecycle management. |
| H1 |
Regulatory Affairs |
| H2 |
Pharmaceuticals Expertise |
| /new-market-authorization-ind-nda-anda-bla: | |
|---|---|
| Title |
IND, NDA, NDS, ANDA Submissions, Applications, Market Authorizations |
| Description |
Freyr helps in filing submission of applications like CTA, NDA, IND, ANDA, 505 b(2), MAAs, NDS, ANDS to comply with US FDA, EMA, EDQM, TPD, PMDA, TGA, MCC for Generics/Biosimilars, Medical Devices, API/Bulk Drugs, OTC, Consumer Healthcare companies |
| H1 |
New Product Authorization - Finished Products |
| H2 |
Pharmaceuticals Expertise |
| H3 |
Freyr Regulatory Consultation and Pre-Submission Support (Sample activities / expertise) |
| /initial-submissions-dmf-asmf-cep: | |
|---|---|
| Title |
DMF, ASMF, CEP Application, Submission, eCTD, USFDA, EMA |
| Description |
Freyr offers compilation, submission services in eCTD format for applications like Drug Master Files (DMF), Active Substance Master File (ASMF), certificate of suitability (CEP) to comply with US FDA, EMA, TPD, TGA, EDQM, MCC, MoH for Pharmaceutical /biological companies. |
| H1 |
New Market Authorizations - APIs |
| H2 |
Pharmaceuticals Expertise |
| H3 |
|
| /regulatory-change-and-lifecycle-management: | |
|---|---|
| Title |
Pharma Lifecycle Management, Variations filing, Gap ysis, Approvals [censored]
|
| Description |
Freyr offers Pharma Lifecycle management which include Post Approval Changes, Core dossier Re-registration & compilation, variations filing, Regulatory Gap ysis, Pre-submission meetings, , Renewal filing for Marketing Authorization Application (MAA), Annual Report filings in eCTD format for Pharma/Biological companies. [censored]
|
| H1 |
Post Approval - CMC and Life Cycle Management |
| H2 |
Pharmaceuticals Expertise |
| H3 |
Post Approval Changes |
| /regulatory- [censorship] essment-Gap- [censorship] ysis: | |
|---|---|
| Title |
Regulatory Gap ysis, essment, CTD Dossier Preparation, Compilation [censored]
|
| Description |
We offer Regulatory essment/Gap ysis for Pharma, Biological companies which spans across CTD Dossier Preparation, Core dossier compilation, CMC Regulatory Affairs support, Drug license renewal applications, Re-registration dossiers, change control evaluation, Pharma supplements/amendments & variations filing [censored]
|
| H1 |
Regulatory essment and Gap ysis [censored]
|
| H2 |
Pharmaceuticals Expertise |
| H3 |
Initial Submissions |
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