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.

09 Sep 2022
Admin
News Article

Us Fda Grants Breakthrough Therapy Designation To Pfizers Gbs Vaccine Candidate To Help Prevent Infection In Infants Via Immunization Of Pregnant Women

Pfizer Inc. Announced That Its Investigational Group B Streptococcus (Gbs) Vaccine Candidate, Gbs6 Or Pf-06760805, Received Breakthrough Therapy Designation From The Us Food And Drug Administration (Fda) For The Prevention Of Invasive Gbs Disease Due To The Vaccine Serotypes In Newborns And Young Infants By Active Immunization Of Their Mothers During Pregnancy.The Fda Decision Is Informed By The Interim Analysis Of A Placebo-Controlled Phase 2 Study (Nct03765073), Evaluating The Safety And Immunogenicity Of Gbs6 In Healthy Pregnant Women Aged 18 To 40 Years, Who Were Vaccinated During The Second Or Early Third Trimester Of Pregnancy. The Study Remains Ongoing, And Pfizer Will Publish Outcomes From This Clinical Trial When It Is Completed.

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