1. What is the Chemxpert database?

Chemxpert database is a techno-commercial information platform developed and operated by Lifescience Intellipedia Pvt. Ltd. Our data provides valuable insights regarding sourcing, marketing, development, and regulatory functions for the entire Lifescience industry. The different industries covered by our data encompass APIs, FDFs, pharma intermediates, paints, dyes, polymers, biotechnology, biochemical, food additives, nutraceuticals, etc.

2. How can I subscribe to the Chemxpert database?

You can gain access to the Chemxpert database after subscribing to it by visiting this link: - https://chemxpert.com/pricing

3. How many countries' data is available on your portal?

The Chemxpert database covers more than 200 countries. We are working in the direction of expanding our data coverage in more countries.

4. What are the different sources you use for obtaining information?

The different sources we use for data collection are as follows: - • Primary researc • DMF, ANDA, & CEP list • Conferences, Exhibitions, & Tradeshow • Company annual reports • DMF, ANDA, & CEP list • Subject matter experts & KOL survey. Apart from these, our other valuable sources include application-wise manufacturers list, subscribed and non-subscribed databases, corporate partners, US FDA Orange book, publicly available sources, industry associates, national statistics, regulatory websites, etc. You can gain access to the Chemxpert database after subscribing to it by visiting this link: -https://chemxpert.com/sources

5. What is the expected time for account activation?

Your Chemxpert account will be activated instantly if the payment is made through our website. If you choose to use RTGS, NEFT, or IMPS systems for payment, your account will be activated within 24 hours.

15 Sep 2022
Admin
News Article

Us Fda Grants Breakthrough Device Designation For Curvebeam Ai S Ossview Bone Fragility Software

Curvebeam Ai Ltd Announced Its Medical Diagnostic Software, Ossview, Has Received Us Food And Drug Administration (Fda) Breakthrough Device Designation. Ossview Calculates A Structural Fragility Score (Sfs), Which Determines Bone Microstructural Deterioration, A Highly Accurate Indicator For Bone Fragility And Fracture Risk.Ossview Is Investigational Only And Is Not Available For Sale In The United States.The Goal Of The Fda Breakthrough Devices Programme Is To Provide Patients And Health Care Providers With Timely Access To Medical Devices That Provide For More Effective Treatment Or Diagnosis Of Irreversibly Debilitating Diseases By Speeding Up Their Development, Assessment, And Review, While Preserving The Statutory Standards For Premarket Approval.Benefits Associated With Acceptance Into The Breakthrough Devices Programme Include Prioritized Review Of Fda 510(K) Applications.The Current Standard Of Care To Determine Fragility Fracture Risk In Patients Is Bone Mineral Density (Bmd) Measurements Obtained Via Dual Energy X-Ray (Dxa). In Some Cases, The Fracture Risk Assessment Tool (Frax) Software Is Used To Further Identify Fracture Risk. These Approaches Miss Patients Who Are Non-Osteoporotic But Still At Risk For Fragility Fracture

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