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 Apr 2023
Admin
News Article

Genenta Science Announces Extension Of Licence Agreement With Ospedale San Raffaele

Genenta Announced That The Licence Agreement With Ospedale San Raffaele (Osr) Has Been Amended And Restated To Provide Access To All Solid Tumour Indications, Subject To Governmental Consent As Described Below.This Agreement Will Strengthen The Breadth Of Ip Position And Confirm Options For Combination Treatments And Other Potential Payloads. Promising Preliminary Clinical Data Generated In The Ongoing Study Of The First Solid Tumour Indication In Glioblastoma Supports Decision To Expand The Licence To Cover All Solid Tumours And Primes Ability To Impact Other Hard-To-Treat Cancer Types.The Amended And Restated Licence Agreement Reinforces Genenta'S Long-Term Strategic Relationship With Osr, Contributing To The Unique And Valuable Expertise For The Development Of Cell-Based Therapies

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