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.

27 Apr 2023
Admin
News Article

Us Fda Grants Accelerated Approval For Qalsody To Treat Als In Adults Who Have A Mutation In Sod1 Gene

Biogen Inc., A Leading Global Biotechnology Company, Announced That The Us Food And Drug Administration (Fda) Has Approved Qalsody (Tofersen) 100 Mg/15Ml Injection For The Treatment Of Amyotrophic Lateral Sclerosis (Als) In Adults Who Have A Mutation In The Superoxide Dismutase 1 (Sod1) Gene. This Indication Is Approved Under Accelerated Approval Based On Reduction In Plasma Neurofilament Light Chain (Nfl) Observed In Patients Treated With Qalsody. Continued Approval For This Indication May Be Contingent Upon Verification Of Clinical Benefit In Confirmatory Trial(S). The Ongoing Phase 3 Atlas Study Of Tofersen In People With Presymptomatic Sod1-Als Will Serve As The Confirmatory Trial.Neurofilaments Are Proteins That Are Released From Neurons When They Are Damaged, Making Them A Marker Of Neurodegeneration.

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