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.

06 May 2020
Admin
News Article

Alembic Pharma Gets VAI Classification From USFDA For Its Panelav Facility

Drug firm Alembic Pharmaceuticals on Monday said the US health regulator has classified inspection of its Panelav manufacturing facility in Gujarat as voluntary action indicated (VAI). The inspection of the company's general oral solid formulation facility at Panelav by the United States Food and Drug Administration (USFDA) was conducted from March 9-13, 2020, Alembic Pharmaceuticals said in a filing to the BSE.The USFDA has classified the inspection as VAI, it added.As per the USFDA, VAI classification means that though objectionable conditions or practices were found, the agency is not prepared to take or recommend any administrative or regulatory action.Shares of Alembic Pharmaceuticals Ltd on Monday closed 1.01 per cent higher at Rs 753.50 on the BSE.

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