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.

08 Apr 2022
Admin
News Article

Novartis Expands Zolgensma Manufacturing Capacity With Approval Of Multi-Product North Carolina Facility

Novartis Announced The Us Food And Drug Administration (Fda) Has Granted Commercial Licensure Approval For Its Durham, North California Site, A Multi-Product Gene Therapy Manufacturing Facility. This Approval Allows The State-Of-The-Art, 170,000 Square-Foot Facility To Make, Test And Release Commercial Zolgensma, As Well As Produce Gene Therapy Product For Current And Future Clinical Trials.The Clearance Of This Milestone Brings Online The Second Commercially-Licensed Manufacturing Facility For Novartis Gene Therapies, Joining The Libertyville, Ill. Site, Which Was Approved For Zolgensma (Onasemnogene Abeparvovec) Manufacturing And Distribution In 2019. The Durham Site Will Build On Novartis Gene Therapies

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