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.

31 May 2022
Admin
News Article

United Biopharma Gets Taiwan Fda Nod For Phase 2 Ind For Ub-221 To Treat Chronic Spontaneous Urticaria

United Biopharma (Ubp), A Taiwan-Based Late Clinical-Stage Biopharmaceutical Company, Has Announced The Approval Of A Phase 2 Clinical Trial With Novel Anti-Ige Monoclonal Antibody Ub-221 By The Taiwan Food And Drug Administration (Tfda).This Phase 2 Clinical Trial (Double-Blind, Placebo-Controlled) Aims To Evaluate The Efficacy Of Ub-221 As A Long-Acting Add-On Therapy For Treatment Of Chronic Spontaneous Urticaria (Csu) And Provide Evidence Of The Therapeutic Potential Of Two High-Dose Ub-221 Treatments Over A 6-Month Period.Spontaneous Urticaria Is Categorized Into Acute ( Six Weeks) Variants. With An Incidence Rate Of 0.5

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