Consulting Services

Thépenier Pharma & Cosmetics provides regulatory affairs support to help partners ensure compliance across pharmaceutical and cosmetic markets. From dossier preparation to coordination with authorities, our team helps ensure GMP-aligned and market-appropriate documentation for domestic and interna...

As part of our QP services and our pharmaceutical consulting, we offer you comprehensive monitoring and assurance of product quality in accordance with the Good Manufacturing Practice (GMP) guidelines and the specific requirements of § 13 AMG. We provide the following services:
• Setting up your Q...

Contract analyticsDevelopment of analytical methods (chromatography – dissolution – particle analysis – titration – wet chemistry)
Formulation screening and compatibility testing for product development
Biopharmaceutical characterization
Specialized analytical methods – special analyses
GMP or ...

Ultra Filter System is applied in downstream purification and separation of biological products, removal of endotoxins in injections, desalination of small nucleic acid products, and solvent removal in the peptide industry, it can provide concentration and liquid exchange functions, as well as clarif...

EU GMP / EU GDP Auditing, Consultancy and Training
We support pharmaceutical manufacturers and supply chain partners in achieving and maintaining compliance with EU regulatory requirements. Our services strengthen quality systems, improve inspection readiness and support sustainable GMP / GDP complian...

As a Managed Service Provider, Catalyx delivers dedicated GMP-expert teams to execute defined scopes of work or support critical functions within a client’s business. Led by an experienced team lead, our solutions ensure full alignment with client expectations while providing managed, flexible, and scalabl...

Blow-Fill-Seal is the most economical way to get your liquids or semi-solids into the perfect shape. But investing in your own equipment doesn't always pay off. For these cases, there is our CDMO service. This means that you have a complete GMP infrastructure, bottelpack technology in various configuration...

Through our partnership network, you gain access to enhanced services and support along the entire device value chain, ensuring smoother processes and better results for your projects.
• Primary packaging • CDMO and CMO • Patient education • Consulting • Digital  

Intertek design audit and action plans to meet the requirements of pharmaceutical clients to ensure compliance with EC standards, FDA regulations and WHO concerns. During a pharmaceutical audit process, Intertek takes a "snapshot" of the company's existing quality system, and superimposes it on the referen...

Global Medicine Database Platform
Pharma14 provides tools for pharmaceutical professionals to monitor registered medicines in 75 countries and guide strategy confidently and efficiently.
Our data includes Rx and OTC medicines, ex-factory, wholesale, retail and tender pricing, daily shortages, rei...

As part of its commitment to full service support, PLD Pharma Services is pleased to offer our customers support with ANDA and NDA applications, including bio equivalency studies, collecting background data, supervising technology tranfers and reviewing applications to make sure that companies comply ...

ArabMed CRO is renowned for its expertise in conducting clinical trials across all phases, from Phase I to Phase IV, with a strong track record in drug research. The company also excels in medical device clinical investigations, demonstrating its commitment to advancing medical technologies. With a focus o...

Finding a right source meeting your desired specifications, compliance, expectations and commercial viability is a challenge.

To support you in bringing even safer medicines to the market, we go far beyond supplying you with the right reference standards. From impurity profiling and working standards outsourcing services, all the way to managing inventory and logistics of your reference standards, we’re fully equipped to provide ...

Condair Esco is a pure steam humidifier which injects plant supplied pure steam through 100% leak-proof stainless steel control valve with stainless steel steam distributors. Condensate is continuously drained from the steam distributors to prevent microbial contamination in the air stream.

Due to recent regulatory developments concerning raw materials, suppliers, manufacturing and distribution, auditing has become a task of critical importance for Life Science businesses.PQE Group supports Pharma and MD companies in performing many types of certified audits, from routine monitoring to due di...

Our Drug Development Consultants work with you to design and implement successful drug development programs. With industry leading scientific expertise across a range of technical disciplines, we help customers across all stages of development, from candidate selection to commercial launch.

Our cons...

Our in-house Industrial R&D Center with over 80 specialists, provides advanced support for optimizing pharmaceutical processes. We cover the entire plant lifecycle, from design to validation, focusing on critical issues such as rouging, leakage, sterility failures, material wear, and malfunctions.Using...

Wilmington PharmaTech offers discovery chemistry services to support early-stage drug development, enabling rapid design, synthesis, and optimization of novel small molecules. The team collaborates closely with clients to advance hit-to-lead and lead optimization programs, focusing on improving potency, se...

deRISC is Mantias’ modular intelligence platform for pharmaceutical supply chain resilience. Built on a digital twin of global manufacturing and supply networks, it enables continuous risk sensing, helping our customers detect vulnerabilities, understand dependencies, and assess concentration risks across ...