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.

08 Sep 2022
Admin
News Article

Fda Grants Breakthrough Therapy Designation To Pfizer'S Group B Streptococcus Vaccine Candidate

Pfizer Inc. (Nyse:Pfe) Today Announced That Its Investigational Group B Streptococcus (Gbs) Vaccine Candidate, Gbs6 Or Pf-06760805, Received Breakthrough Therapy Designation From The U.S. 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."Gbs Infections Can Have A Devastating Effect On Newborns And Their Families. While Prenatal Screening And Antibiotics During Childbirth Help Provide Protection Against Gbs In Developed Countries, This Approach Is Not Fully Protective In The First Week Of Life; Presents Multiple Challenges In Low- And Middle-Income Countries; And Has Not Been Shown Effective In Preventing Disease Globally In Infants Beyond The First Week Of Life And Through The Vulnerable First Three Months Of Life," Said Annaliesa Anderson, Ph.D., Senior Vice President And Head Of Vaccine Research & Development, Pfizer. "If Approved For Pregnant Women, Gbs6 Could Help Protect Newborns From The Serious Illnesses Caused By This Disease Like Meningitis, Pneumonia, And Sepsis - Fulfilling A Critical Global Public Health Need. We Are Encouraged By Today

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