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.

07 Apr 2022
Admin
News Article

Novartis Vijoice Gets Us Fda Accelerated Approval For Select Patients With Pik3Ca-Related Overgrowth Spectrum

Novartis Announced That The Us Food And Drug Administration (Fda) Granted Accelerated Approval To Vijoice (Alpelisib) For The Treatment Of Adult And Paediatric Patients 2 Years Of Age And Older With Severe Manifestations Of Pik3Ca-Related Overgrowth Spectrum (Pros) Who Require Systemic Therapy. Vijoice Is The First Fda-Approved Treatment For Pros, A Spectrum Of Rare Conditions Characterized By Overgrowths And Blood Vessel Anomalies Impacting An Estimated 14 People Per Million. In Accordance With The Accelerated Approval Programme, Continued Approval May Be Contingent Upon Verification And Description Of Clinical Benefit From Confirmatory Evidence.

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