Data services

A little about Pharma14.

The Pharma14 database platform covers 70 countries and deals in the tracking of finished dosage formulations as well as business analysis tools.

Our data has all registered medicines, prices, consumption data, reimbursement data and much more.
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Cortellis Product Intelligence is a comprehensive source of global drug, market, API, and patent data that helps innovators, CDMOs, generics and API manufacturers grow their business and build robust supply chains.

Lomapharm GmbH provides wide range of services which includes approvals and registration. One can benefit from the long experience with a large range of pharmaceuticals and their preparation, including analysis. From analysis to approvals: We are a competent partner for solid, liquid and sterile produc...

You need data rapidly to make crucial decisions during a study. Faster data means we can provide our customers with earlier interim data and interim PK reports for on-study dosing and formulation decisions.
We understand on-study changes to early phase study designs and d...

Res_Q helps IT and quality leaders eliminate validation debt, achieve peace of mind and untangle valuable resources. Res_Q's data-focused architecture and wide array of industry-supported applications prevent you from falling deeper into validation debt with every new software release.

Unify is our Contextualized Intelligent Lakehouse: Streamline pharma manufacturing analytics by integrating your data across your processes, systems and sites and leveraging solutions made for the industry.

Formula and Label Assessment:In-depth review of product formulas and labels to ensure compliance with local regulatory requirements
⁠Identification of the regulatory authority and correct product category to be registered
Market Analysis (Online retail, or Amazon/Noon Separately, or Online + Off...

OP Pharma has been providing all-around services in the Regulatory Affairs field for more than 20 years to small to big pharma Companies in Italy as well as in the European Union.
Our expertise ranges from submission of registrations, variations, prices, texts, renewals (also via CESP), to CEP and...

With new advanced technologies and new standards for Compliance and Cybersecurity, developing an intelligent network and infrastructure is a top level priority for Life Science businesses. Choose PQE Group’s all-in-one integrated solutions to coordinate your Corporate Digital Development.

Gaining a competitive edge in drug development requires monitoring the current pipeline while keeping an eye to the future. Cortellis Competitive Intelligence™ delivers timely intelligence to survey the entire development landscape and provides comprehensive analysis to forecast trends, threats and opportu...

Cortellis CMC Intelligence™ product is a comprehensive database of guidelines / granular collection of CMC data requirements for initial registration of small-molecule and biologics drugs around the world that can be used to avoid delays in product approval and successfully bring a drug to the market (laun...

Navigate the regulatory landscape and efficiently drive strategic decisions with Cortellis Regulatory Intelligence. Get full and timely coverage of global health authority requirements on healthcare products such as drugs, biologics, medical devices and IVDs, and access exclusive expert reports for both in...

Biology, chemistry and pharmacology data –all in one place. Cortellis Drug Discovery Intelligence™ can help fine chem manufacturers and custom synthesis organizations grow their business by finding and prioritizing new opportunities:

-Access integrated chemistry, organic synthesis and drug pip...

Benefit from the industry's highest quality and largest deals database. Effective deal making is crucial for company growth, getting drugs/devices to market and overall commercial success. Cortellis Deals Intelligence™ provides the essential data foundation to quickly find the most optimal deal without com...

Increase successful submission outcomes in markets worldwide with comprehensive, expertly analyzed regulatory and market access information: 

-Get treatments to patients faster Compare and monitor regulations quickly across markets to understand regional health technology assessment (H...

Confidently and efficiently plan and design clinical trials by reducing time spent compiling and analyzing protocols, sites, outcomes, endpoints and more. Avoid costly protocol amendments, recruitment delays and trial failure by tracking competitive trials, selecting experienced sites, defining the right e...

Keep up to date with regulations, maintain biopharma regulatory compliance and make the right strategic decisions. 

Navigate the regulatory landscape and efficiently drive strategic decisions 

-Comprehensive repository of pharma regulatory intelligence Get full and time...

Monitor and anticipate toxicology and safety signals, mitigate safety liabilities and de-risk assets across all phases of drug R&D and post-marketing. 

Make confident development and investment decisions with comprehensive translational safety intelligence. OFF-X™ provides integrated pr...

Cortellis CMC Intelligence product is a comprehensive database of guidelines / granular collection of CMC data requirements for initial registration of small-molecule and biologics drugs around the world that can be used to avoid delays in product approval and successfully bring a drug to the market (launc...

Increase successful submission outcomes in markets worldwide with comprehensive, expertly analyzed regulatory and market access information 1. Get treatments to patients faster Compare and monitor regulations quickly across markets to understand regional health technology assessment (HTA) outcomes. 2. Main...