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 Jul 2022
Admin
News Article

Dr Reddys Laboratories Says Its Andhra Plant Gets Two Observations From Usfda

The Us Food And Drug Administration (Usfda) Completed A Pre-Approval Inspection At The Company'S Formulations Manufacturing Facility Fto 11 In Srikakulam, Andhra Pradesh On Thursday, Dr Reddy'S Said In A Regulatory Filing. The Inspection Was Conducted From June 30, 2022 To July 7, 2022Dr Reddy'S Laboratories Ltd On Thursday Said The Us Health Regulator Has Issued Form 483 With Two Observations After Inspecting Its Manufacturing Facility Located At Srikakulam In Andhra Pradesh. As Per Usfda, Form 483 Is Issued To A Firm'S Management At The Conclusion Of An Inspection When The Investigator Has Observed Any Conditions That In Its Judgment May Constitute Violations Of The Food Drug And Cosmetic (Fd&C) Act And Related Acts. The Us Food And Drug Administration (Usfda) Completed A Pre-Approval Sirkakulam, Andhra Pradesh On Thursday, Dr Reddy'S Said In A Regulatory Filing. The Inspection Was Conducted From June 30, 2022 To July 7, 2022. "We Have Been Issued A Form 483 With Two Observations, Which We Will Address Within The Stipulated Timeline," The Company Added

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