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.

30 Dec 2020
Admin
News Article

Wuxi Biologics Gets Good Manufacturing Practice Certification From Brazils Anvisa

Wuxi Biologics, A Global Company With Leading Open-Access Biologics Technology Platforms, Announced That It Has Received The Good Manufacturing Practice (Gmp) Certification From Brazil'S AgÊNcia Nacional De VigilÂNcia SanitÁRia (Anvisa). The Positive Assessment From Anvisa Reaffirms Wuxi Biologics' Strong Commitment To Offering Partners A Global Manufacturing Network Of The Highest Standard.This Is Wuxi Biologics' Third Gmp Certification From Drug Regulatory Authorities, And Distinguishes It As The First Company In China To Receive Authorizations From The Us Food And Drug Administration (Fda), European Medicines Agency (Ema) And Anvisa To Manufacture Biologics. To Date, Wuxi Biologics' Facilities In Wuxi City, Shanghai And Suzhou Have Passed A Total Of Six Gmp Inspections Conducted By These Regulatory Agencies."We Are Very Excited To Have Reached Another Regulatory Milestone During This Challenging Year. This Achievement Once Again Demonstrates Wuxi Biologics' High-Quality Services, Which Have Been Widely Recognized By Regulatory Authorities. We Owe This Achievement To Our Partners' Trust In Our Capabilities And Our Team'S Tireless Commitment To Excellence," Commented Dr. Chris Chen, Ceo Of Wuxi Biologics. "As Outsourcing Demand Increases Around The World, We Have Made Huge Strides In Expanding Our Services Globally And Plan To Increase Our Total Biomanufacturing Capacity To 300,000 Liters After 2023. Wuxi Biologics Will Continue To Enable Our Global Partners Throughout The Development And Manufacturing Process To Provide Life-Saving Treatments To Patients Worldwide."Wuxi Biologics, A Hong Kong-Listed Company, Is A Leading Global Open-Access Biologics Technology Platform Offering End-To-End Solutions To Empower Organizations To Discover, Develop, And Manufacture Biologics From Concept To Commercial Manufacturing.

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