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.

21 Sep 2022
Admin
News Article

Wuxi Biologics Drug Substance And Drug Product Facilities Again Approved By Us Fda And Ema

?Wuxi Biologics Leading Global Contract Research, Development And Manufacturing Organization (Crdmo), Today Announced That Its Two Drug Substance (Ds) Facilities And A Drug Product (Dp) Facility Located In Wuxi City Received Regulatory Approvals From The European Medicines Agency (Ema) And The U.S. Food And Drug Administration (Fda).After Passing Online Pre-Approval Inspection (Pai), Wuxi Biologics Received Ema Gmp Certificates For The Commercial Manufacturing Of Two Biologics Developed By Global Clients At Its Mfg4, Mfg5 And Dp2 Facilities. This Is The First Time Mfg5, The Newest Operational Ds Facility With A Total Of 60,000L Capacity, And Dp2, The Second Dp Facility For Vials, Have Been Certified By The Ema, Only 10 Months After They Were Released For Gmp Manufacturing. The U.S. Fda Also Approved Mfg5 To Manufacture An Innovative Product For A Global Client.Dr. Chris Chen, Ceo Of Wuxi Biologics, Commented, "We'Re Proud That Our Additional Ds And Dp Facilities Have Again Been Approved By Both The U.S. Fda And Ema. It Is A Strong Testament Of The Global Quality Standards We Adhere To. We'Ll Continue To Establish Our World-Class Quality System Across All Global Sites To Ensure That Biologics Are Manufactured At The Highest Quality So That We Can Continue To Enable Our Partners With A Robust Supply Chain For The Benefits Of Patients Worldwide."These Approvals Add To The Previous 25 Certifications From More Than 10 Global Regulatory Administrations. So Far, Wuxi Biologics Has 13 Certified Ds And Dp Facilities On A Global Basis.About Wuxi BiologicsWuxi Biologics (Stock Code: 2269.Hk) Is A Leading Global Contract Research, Development And Manufacturing Organization (Crdmo) Offering End-To-End Solutions That Enable Partners To Discover, Develop And Manufacture Biologics

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