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.

10 Jan 2023
Admin
News Article

Frontera Therapeutics Begins Patient Dosing In Phase 1 Trial Of Gene Therapy Ft-001 To Treat Leber Congenital Amaurosis-2

Frontera Therapeutics, A Global Clinical-Stage Biotechnology Company, Announced That It Has Dosed The First Patient In A Phase 1 Clinical Trial Of Its Lead Gene Therapy Programme, Ft-001, For The Treatment Of Leber Congenital Amaurosis-2, A Severe Inherited Retinal Disease Related To A Mutation In The Rpe65 Gene. Ft-001 Is Administered By A One-Time Injection Into The Subretinal Space Of The Eye That Delivers A Functional Copy Of The Human Rpe65 Gene To The Nuclei Of The Patient

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