Consulting Services

Nanomake-L™ is Amar Biosystem’s fully automated microfluidic platform designed for reproducible nanoformulation development, nanoparticle synthesis and advanced drug-delivery formulation. It enables controlled mixing and formulation of lipid nanoparticles (LNPs), liposomes, emulsions and other nanoformulat...

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...

Most organisations face Scope 3 emissions as their largest decarbonization challenge. For many manufacturing, pharmaceutical, and chemical organisations, Scope 3 emissions can account for up to 90% of their total footprint, placing value-chain emissions under increasing regulatory and stakeholder scrutiny....

Specialist AI agents that do formulation development work, end to end. Describe the problem in plain language; DeepC plans the work, routes it to the right specialists and returns decision-ready deliverables in minutes: complete development assessments, excipient selection justified against precedent and t...

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  

In the Life Science industry, robust processes and effective technology management are essential to ensure consistent product quality throughout the product lifecycle. S4BT provides comprehensive Manufacturing Science & Technology (MS&T) support, helping organizations manage, optimize, and validate...

Positive Organizations builds the ESG strategy that sits underneath everything else, so your reporting, ratings and customer questionnaires draw on one coherent plan instead of ad hoc answers.


We begin with an ESG maturity assessment and a peer benchmark against comparable pharmaceutical manufac...

Your Compliance Partner for Drug Development & Product Life Cycle 

PharmSol carries out a complete chain of audits which assures product safety and quality to clients across the globe for Finished Products, APIs, Intermediates and Key Starting Materials (KSMs). PharmSol has an in-house team of Auditors who are accredited with various certifications including APIC/CEFIC/AS...

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...

Over 400 developed recipes, 
including over 30 medical devices in various classes and indications,
in 20 pharmaceutical forms - 
everything starts in the Gofarm's R&D Laboratory.



In Gofarm's R&D Laboratory our and our clients' ideas take real shapes...

We offer research and development services at all stages of the production of capsules, from idea to finished product for medicinal products, medical devices, food supplements, cosmetics and veterinary products.

We offer our clients a proper identification of their needs and requirements, r...

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...

Intertek provides GMP audit services to support pharmaceutical, biopharmaceutical and healthcare companies in assessing, qualifying and monitoring suppliers, manufacturers and service providers across global supply chains. 

Our audits evaluate compliance with applicable Good Manufacturing P...

Biological evaluation plans & reports (BEP & BER) Clinical evaluation plans & reports (CEP & CER) Submission support (US FDA, UK & EU MDR) Toxicological risk analysis Biological gap analysis PSUR (Periodic safety update report) Post market surveillance

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...

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...

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...