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.

Company Data Summary Report Of Merck Eprova Ag

Summary Of Merck Eprova Ag

Download All File (.xls)

Company Name

Merck Eprova Ag

Type Of Company

Manufacturer

Employee Strength

69000

Key Management

Martin Ulmann

Designation

Managing Director

Contact Number

41-52-6307272

Country

Switzerland

Region

Western Europe

Continent

Europe

Certifications/ Accreditation

No Record Found

Competition/Peer

API-Small Molecules

Finished Dosage (FDF)

Pharma Intermediates

Fine & Speciality Chemicals

Financials

FY20-21 Click here

FY21-22 Click here

FY22-23 Click here

Patent Filed

US-Patent Expiry 0

US-Exclusivity

US-SPC 0

US-PARA IV

Warning Letter By Authority

US-FDA Recall

US-FDA Warning

EU-Under Monitoring List

US-FDA Site Inspection

Pipeline Products

Clinical Trial Product 0

Product Under Development 0

North America

US-DMF

FDA-NDC

Europe

CEP/COS

EU-API Registered

EU-Written Conf-India

REACH Registered

UK-MHRA

Asia

J-DMF

K-DMF

India Import Licence

China-API Registered

Egypt-API Registered

North America

US FDA-NDC

US-ANDA

Canada

Cuba

Mexico

US-Excipients

Europe

National Registered

Albania

Spain

Greece

Italy

United Kingdom

Centralised

Centralized Registered

Decentralised

Decentralized Registered

Others

UK Parallel Import Licence

Veterinary Registered

Oceania

Australia

New Zealand

Africa

Nigeria

Cameroon

Ethiopia

South Africa

Tanzania

Ghana

Asia

Nepal

Japan

South Korea

Indonesia

Thailand

Srilanka

Kazakhstan

Egypt

Saudi Arabia

Philippines

Turkey

Vietnam

South America

Brazil

Argentina

Colombia

Ecuador

Peru

Bolivia

Clinical Trial

United States 0
United States 0

Europe 0
Europe 0

Japan 0
Japan 0

Canada 0
Canada 0

Biosimilar

United States

Canada

Argentina

Brazil

Europe

Australia

Japan

South korea

India

China

Malaysia

Cookies & Privacy

This website uses ‘cookies’ to operate our site and personalize your digital experience. By continuing to browse this website, you agree to the terms outlined in our Privacy Policy, Cookies Policy

Summary Of Merck Eprova Ag

BASIC INFORMATION

Company Name

Type Of Company

Employee Strength

Key Management

Designation

Contact Number

Country

Region

Continent

Company URL

VIEW DETAILED ANALYSIS (Click the items for details)

Business Area

Products Portfolio

Buying Portfolio

Subsidiary and Affiliates

Manufacturing Locations

Certifications/ Accreditation

Competition/Peer

Financials

Patent Filed

Warning Letter By Authority

Pipeline Products

Recent News

Regulatory Info (Active Ingredients Filing/Registration/Market Authorization)

North America

Europe

Asia

REGULATORY INFO - (FINISHED DOSAGE FORMS(FDF) FILING/REGISTRATION/MARKET AUTHORIZATION)

North America

Europe

National Registered

Centralised

Decentralised

Others

Oceania

Africa

Asia

South America

Clinical Trial

Biosimilar

Cookies & Privacy

Select cookies to accept