- Service Details

PMC ISOCHEM offers cGMP and non cGMP industrial exclusive custom synthesis and provides tailor made services from development to production, including route selection, process and analytical development as well as process optimization.

- Service Details

Bachem is the world´s leading independent manufacturer of peptide & small molecules APIs. Each year, Bachem manufactures hundreds of batches of drug substance for projects in clinical trials and for products on the market.

- Service Details

ScinoPharm provides chemical synthesis and manufacturing services for our customers under strict US and international cGMP guidelines.

- Service Details

Dishman's CRAMS business offers a range of high-value, cost competitve contract services. It includes process development, process optimization, manufacture for late stage clinical & commercial supply.

- Service Details

Dishman facilities operate to current Good Manufacturing Practice (cGMP) and can produce material for preclinical testing, clinical trials and commercial use. Our manufacturing sites are regularly inspected by the US Food and/or Drug Administration (FDA) and local regulatory bodies.

- Service Details

We have deep experience in helping our clients move forward from the discovery phase of product development to the scale up of New Chemical Entities for clinical supply.

- Service Details

Servier CDMO offers a full range of contract development and manufacturing services, from concept and product development to analytical testing, commercial scale and regulatory approval.

- Service Details

Our kilo lab allows us to conveniently bridge the gap between lab and pilot scale.

- Service Details

Cook Pharmica is a leading contract development and manufacturing organization (CDMO) centrally located in Bloomington, Indiana. From the beginning, Cook Pharmica set out to build a CDMO that would meet and exceed the expectations of the biopharmaceutical industry.

- Service Details

Diverchim has several equipped laboratories with one fully dedicated to cGMP production (clinical phases and recurrent production) for tens of grams.

- Service Details

KriSan Biotech has cGMP manufacturing of API for clinical trials (few grams to kilograms scale)

- Service Details

DOTTIKON's facilities are suited to the manufacturing of chemical intermediates and active pharmaceutical ingredients (APIs) in clinical trials, as well as for marketed small-volume APIs. The small-scale capabilities are equipped to handle high-potency pr

- Service Details

Chemspec Exclusive Synthesisfor Pharma Chemicals focuses on a spectrum of early clinical to commercial services that are aligned with the long-term needs of pharmas and biotechs for small molecule projects.

- Service Details

Fermion develop, manufacture and market APIs for generic, specialty and branded pharmaceutical companies and offer fully integrated contract development and manufacturing services from phase I to commercial scale.

- Service Details

Synthesis of APIs for preclinical and clinical studies up to phase II.

- Service Details

Our custom synthesis business integrates completely all the phases of chemical development: design of a novel synthetic pathway accompanied by supply of a few grams, provision of pilot batches following development of the industrial procedure.

- Service Details

The combination of Indena’s expertise and top class facilities delivers products and processes from small scale GLP batches for toxicology, cGMP batches for clinical trials to large-scale commercial manufacturing.

- Service Details

Farmhispania Group has at both sites pilot plants and kilo-labs to scale up manufacturing processes and carry out cGMP manufacture of API´s for Clinical Trials and commercial supply.

- Service Details

We offer Integrated formulation activities, Clinical manufacturing, Commercial manufacturing of your Drug Substance and Scalability within one single dedicated platform.

- Service Details

Olon's R&D expertise extends over a wide range of areas. It includes: development of synthetic route of new chemical entities; production of GMP material for clinical supply; process improvement activities.