• Freyr Solutions

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  • Regulatory Services in India, CDSCO, Regulatory affairs consulting

    Regulatory Services in India, CDSCO, Regulatory affairs consulting

    Other Services Hyderabad (Andhra Pradesh) October 12, 2021 Check with seller

    Freyr provides regulatory services and solutions in India to comply with CDSCO regulations for pharmaceuticals, medical devices, cosmetics, and food supplements manufacturing companies. https://www.freyrsolutions.in/

  • UK Responsible Person (UKRP), UK Responsible Person Medical Devices

    UK Responsible Person (UKRP), UK Responsible Person Medical Devices

    Health - Beauty - Fitness Hyderabad (Andhra Pradesh) April 28, 2021 Free

    Freyr provides United Kingdom Responsible Person (UKRP) services to foreign medical device manufacturers in product registration and market entry in the UK and acts as a single point of contact in the Country for liaison with Regulatory Agency.

  • Regulatory Solutions and Services in Australia, TGA | Freyr Australia

    Regulatory Solutions and Services in Australia, TGA | Freyr Australia

    Health - Beauty - Fitness Hyderabad (Andhra Pradesh) April 28, 2021 Free

    Freyr Australia provides End-to-End Regulatory Solutions & Services in Australia to the Pharma Innovator, Generics, Biologics, Medical Device, Food Supplements and Cosmetic Companies to comply with TGA Regulations.

  • Brexit Consequences, Regulatory Support, Consulting

    Brexit Consequences, Regulatory Support, Consulting

    Health - Beauty - Fitness Hyderabad (Andhra Pradesh) April 28, 2021 Free

    Freyr provides End-to-End Post Brexit regulatory support for Pharma, Medical Devices, Cosmetics and Food Supplements manufacturers who are willing to market their products in United Kingdom (UK) and EU.

  • Medical devices regulatory services, medical device registration, IVD classification

    Medical devices regulatory services, medical device registration, IVD classification

    Health - Beauty - Fitness Hyderabad (Andhra Pradesh) April 28, 2021 Free

    Freyr provides end to end regulatory support for medical device & IVD manufacturers in product registration, notification, classification across the globe.

  • Best eCTD Software Tool for global eCTD Submissions

    Best eCTD Software Tool for global eCTD Submissions

    Computer Hyderabad (Andhra Pradesh) April 28, 2021 Free

    Freyr SUBMIT Pro is one of the best eCTD software tool which helps Life science companies in various regulatory submissions to global health Authorities.

  • Artwork Management System, Product lifecycle management, PLM Tool

    Artwork Management System, Product lifecycle management, PLM Tool

    Other Services Hyderabad (Andhra Pradesh) March 31, 2021 Check with seller

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

  • Structured Product Labeling, SPL Software, SPL Format | Freyr SPL

    Structured Product Labeling, SPL Software, SPL Format | Freyr SPL

    Other Services Hyderabad (Andhra Pradesh) March 31, 2021 Check with seller

    Freyr SPL/SPM tool is an easy to use SPL/SPM Software that manages SPL/Pharma listing lifecycle & validates the output as per USFDA regulations with seamless SPL Submissions.

  • Pharmaceutical Labeling Software, Regulatory Labeling Management

    Pharmaceutical Labeling Software, Regulatory Labeling Management

    Other Services Hyderabad (Andhra Pradesh) March 31, 2021 Check with seller

    Freyr label 360 is a Pharmaceutical Labeling Software that Supports End to End Label Management, Label Tracking and Deviation Management for Pharmaceutical Companies across the Globe.

  • Artwork Management Services, Artwork Solutions, Life Sciences

    Artwork Management Services, Artwork Solutions, Life Sciences

    Other Services Hyderabad (Andhra Pradesh) February 26, 2021 Check with seller

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


Frequently Asked Questions (FAQ) ✅

1. Is Registration necessary Before Posting a Classified Ad?

Yes, the Registration is necessary before posting an ad on Top Classifieds 4 U portal. You can register with your email id or social logins such as Google+, Facebook or Twitter. After login into the Top Classified account, you can easily post an ad by filling the necessary details.

2. What is the process of Posting a Classified Ad?

You have to register before posting a classified ad. After Registration, you have to login into the account and click on Publish Classified Ad. You have to fill the form which contains the title, description, image, contact details and so on. After filling all the necessary details, you have to pay a nominal amount of INR 100 to get your ad activated at Top Classified 4 U Portal.

3. What is the Charge of Placing a Classified Ad on Top Classifieds 4 U?

Our Websites is High DA 53+ PA 40+ Classifieds. There is a nominal amount we are charging for the classified Ads. The nominal amount is INR 100, which is the least amount. The amount charged is due to avoid the spam content and to enhance the genuine users to promote their business and services at Classified portal.

4. What Form of Payment are accepted at Top Classifieds 4 U?

As we are accepting a nominal charge of INR 100 for accepting the classified ads, we are having different forms of payment mode. You can either pay from a debit or credit card. You can use your net banking too or pay the amount from BHIM UPI ( Google Pay, PhonePe, Paytm, etc.). Select any of the option to pay the nominal charge for classified Ads.

5. How Long Will It Take to My Ads Approved?

Generally, it takes 1-2 hours for accepting the classifieds ads. There are many categories in which you can post the classified ads. You can promote the business and services by posting an ad on Top Classifieds 4 U portal. Gambling, Adult and Medical related Ads are prohibited. Your ads must be unique and properly written to get it approved.



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