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.

28 Feb 2020
Admin
News Article

Usfda Issues Warning Letter To Cipla For Goa Manufacturing Facility

Drug Firm Cipla Ltd On Wednesday Said That The Us Health Regulator Has Issued A Warning Letter To The Company For Its Manufacturing Facility In Goa."Further To Our Earlier Communication On The Goa Manufacturing Facility Inspection Conducted From September 16-27, 2019 By The United States Food And Drug Administration (Usfda), The Company Has Received A Warning Letter From Usfda," Cipla Ltd Said In A Regulatory Filing.The Company Further Said That It Remains Committed To Maintain Highest Standards Of Compliance And Will Work Closely With The Agency To Comprehensively Address All The Observations.Shares Of Cipla Were Trading At Rs 418.30 A Piece On Bse In The Morning Trade On Bse, Down 1.66 Per Cent From Its Previous Close.

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