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.

25 Jun 2022
Admin
News Article

Us Fda Granted Accelerated Approval To Novartis Tafinlar + Mekinist For First Tumour-Agnostic Indication For Braf V600E Solid Tumours

Novartis Announced The Us Food And Drug Administration (Fda) Granted Accelerated Approval For Tafinlar (Dabrafenib) + Mekinist (Trametinib) For The Treatment Of Adult And Paediatric Patients 6 Years Of Age And Older With Unresectable Or Metastatic Solid Tumours With Braf V600E Mutation Who Have Progressed Following Prior Treatment And Have No Satisfactory Alternative Treatment Options. In Accordance With The Accelerated Approval Programme, Continued Approval For This Indication May Be Contingent Upon Verification And Description Of Clinical Benefit In A Confirmatory Trial(S). Tafinlar + Mekinist Is The First And Only Braf/Mek Inhibitor To Be Approved With A Tumour-Agnostic Indication For Solid Tumours Carrying The Braf V600E Mutation, Which Drives Tumour Growth In More Than 20 Different Tumour Types, And It Is The Only Braf/Mek Inhibitor Approved For Use In Paediatric Patients.

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