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.

09 Sep 2019
Admin
News Article

Tagrisso Approved In China As A 1St-Line Treatment For Egfr-Mutated Non-Small Cell Lung Cancer

Astrazeneca Today Announced That It Has Received Marketing Authorisation From China'S National Medical Products Administration (Nmpa) For Tagrisso (Osimertinib) As A 1St-Line Treatment For Adults With Locally-Advanced Or Metastatic Non-Small Cell Lung Cancer (Nsclc) Whose Tumours Have The Genetic Mutations Of Epidermal Growth Factor Receptor (Egfr) Exon 19 Deletions Or Exon 21 (L858R) Substitutions.The Approval Followed The Priority Review Pathway And Is Based On Results From The Phase Iii Flaura Trial, Which Were Published In The New England Journal Of Medicine.Dave Fredrickson, Executive Vice President, Oncology, Said:

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