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Packaging services of powder (status: medicinal product) into glass bottles

  • Contract manufacturing, filling and packaging
  • Human Medicines
  • Europe

Looking for a company offering packaging services of powder (status: medicinal product) into glass bottles of 250 ml, 125 ml, 100 ml. More »

Biopharma searches expertise in in silico drug design/target matching for inorganic compounds

  • Pharmaceutical process development and validation
  • Human Medicines
  • Worldwide

We look for experts providing access to SAR knowledges (ligands, in silico,...) for inorganic metal-based small molecules. From a pool of actual compounds having demonstrated in vitro activity and identified molecular pathways, we want: - identifi... More »

Start-up looks for redox enzymes assay screening

  • Pre-clinical development and testing, pre-clinical CRO
  • Human Medicines
  • Worldwide

As it exists for kinases, we're looking for CRO providing in vitro testing on a panel of redox enzymes and redox molecular targets to screen small molecules. Please indicate estimated cost and timing for 5-10 candidates. More »

Paracetamol Infusion License

  • Partnering/collaboration for drug dossiers, patents, drug candidates, medical technology
  • Generics
  • Europe

Looking for a European Licence holder to supply Paracetamol Infusion for Export into other non-EU Markets More »

Looking to license products for import to China

  • Consulting - strategy and development
  • Human Medicines
  • Europe, North America, Australia & New Zealand

We are a 30 year old US company with assets in China. Our pharma division licenses late stage and commercially marketed products from regulated markets to register and import to China. We are looking for quality pharma products and medical devices in... More »

Director Business Development

  • Contract manufacturing, filling and packaging
  • Human Medicines
  • Europe, North America

Setting up Joint Venture for manufacture of Oncology Products in Saudi Arabia with transfer of technology for supply to regional markets More »

Regulatory support for 510K and CE mark process for a new laboratory standard

  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • Europe, North America

We need support to identify the requirements each of the sites involved in the manufacture, release and distribution of the standard must comply with for the step they are involved in the process. Later we may also need advice on the documentation ... More »

Levodopa-induced dyskinesia model in MPTP-marmosets

  • Pre-clinical development and testing, pre-clinical CRO
  • Human Medicines
  • Worldwide

We are looking for CRO's routinely performing levodopa-induced dyskinesia studies in MPTP-primed marmosets. Good experience with the model and reference data is a plus. More »

Clinical CRO with specialisation in oncology for Phase I in patients

  • Clinical development and testing, clinical CRO
  • Human Medicines
  • Europe

We look for a clinical CRO specialised in breast cancer. A neoadjuvant study design is planned to be used in a Phase I in postmenopausal patients with breast cancer (>T2). More »

Search for a global CRO that can devise a strategy of running a series of pediatric trials in the pain indication.

The CRO should take into consideration synergies and potential overlaps in terms of patient population age groups, indications, the benefit of using the same trial sites repeatedly or performing the trials in parallel. More »

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