Project Management

Recipharm offer formulation development services for all dosage forms. We develop everything from simple formulations for early studies to more complex formulations suited for commercialisation.

Navigating both general and country-specific regulations and requirements to supply medicinal products to the European markets can be a complex challenge for Marketing Authorization Holders (MAH). ProPharma holds both EU and UK MIA licenses which allows us to help clients overcome the complexities of su...

Global Verification & Validation is a SaaS solution for Life Science companies that complies with EMA/FDA. FIVE Validation developed a SaaS platform that allows AI and traditional validation studies to proceed 6x faster than a manual (electronic or paper-based) process.

Safeguard patient health with our next-generation Betabags.
Our range of next-generation Betabags brings significant improvements to sterility assurance and operator ergonomics. Designed specifically for parenteral products applications, our Betacleanbags® can be used for many more.

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With a team of experienced scientists and a robust toolbox of analytical techniques and equipment, Experic can support the life cycle of your oral solid dose and/or inhalation pharmaceutical products. Our laboratory staff provides comprehensive analytical solutions to support the formulation, development, ...

IGB Ampoule Trays are entirely madeof cardboardThey are safe, eco-friendly and easyto us
They are made by a state-of-the-artmachine, designed by IGB: unique inItaly and most advanced in Europe.
The trays are ideal for the packagingof pharmaceutical and cosmetic vialsand ampoules

The Investment and Development Agency of Latvia (LIAA) is a direct administration institution subordinated to the Minister of Economics of the Republic of Latvia. LIAA supports companies in Latvia trading internationally as well as overseas enterprises seeking business partners in Latvia. LIAA promote...

Avivia offers full product development services to generic drug companies and specialty pharma focused on the development of new improved versions (value-added generics or generic plus) of established drug products.
Although in general the overall aim of value-added generic development projects is focu...

State-of-the-art phase I/ll unit supporting complex clinical trials • First in Human ( FIH) to Proof of Concept ( PoC) • Clinical pharmacology studies through all phases • In-house safety lab and bioanalytical services • Special patient populations (with a focus on respiratory) • Data m...

Our new BA100 blister packaging line.

PharOS Ltd. offers a wide range of services which includes business development. Features: it provides new opportunities and growth potential to clients. The experienced managers continuously seek, identify and assess individual products and potential new markets. The broad network of professionals, locate...

From early-stage development through commercial support, our experts provide critical GxP-based consulting services. We partner with clients to successfully execute projects throughout the product lifecycle to maintain quality & compliance with applicable regulations and industry standards. qq...

Our range of rapid transfer ports, ABC Transfer’s Alpha Ports, ensure safe sterile and aseptic transfers for isolator systems in pharmaceutical filling lines. Our Alpha ports, rapid transfer port are compatible with other brands and fully comply with the Annex 1 of the European GMP.

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Young children are curious by nature and always up todiscovering new things. Children often get poisonedbecause they find dangerous products at their reachand they simply do not know they are harmful. Childresistant packaging is a key prevention device.The IGB CR cartons are made of a tear-resistant,100% p...

Recipharm offer a range of synthetic chemistry services through our global development facilities including advanced lead optimisation medicinal chemistry, process development and tech transfer to large scale GMP-manufacturing and other specialties.

Recipharm offer analytical support for drug discovery, pharmaceutical development and manufacturing through our global development facilities.

Recipharm have more than 20 years experience supplying clinical trial material to our clients. Our development facilities cater for a range of clinical trials from preclincal to smaller Phase III trials. We also offer commercial manufacturing for very large clinical batches.

We provide design, supply, installation, commissioning of clean room according to different regulatory guidelines. We provide clean room according to different class grade like A,B,C,D,CNC.

The Clinvigilant eClinical suite includes: EDC, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them with your existing software ecosystem.

Clinvigilant is a global cost-effective eClinical tools provider for Pharma, Biot...

Our experts will accomplish your clinical objectives by leading the way from recruitment strategies, site selection, and clinical logistics, all the way through the regulatory process. 

We use our own eClinical suite to be more cost-efficient and keep you connected remotely acros...