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Looking for finished product files

  • Contract manufacturing, filling and packaging
  • Human Medicines
  • Europe, South America, Worldwide

We are looking for finished product files for Ivabradine, Bosentan and Flucanazole. Actually if you have a list of the companies have finished product file we will contact with them easily. More »

Drug Master File

  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • Asia

Looking for Drug Master file of Hydaralazine Hydrochloride USP More »

Drug Master File

  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • Asia

Looking for Drug Master file of Hydaralazine Hydrochloride USP More »

Looking for regulatory services in UAE

  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • Middle East

We are a drug store in UAE, looking for outsource regulatory affairs, who can help in the registration of new products in ministry of health in UAE. More »

Looking for EU-CTD Dossier for nicotine lozenge

  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • Europe

We are looking for EU-CTD dossier with market authorization in some European country or ready-to-file for nicotine lozenge. All strengths and flavors considered. Additional background information will be available for potential providers. More »

Looking for provider for ICH CTD to ACTD conversion

  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • Asia, Worldwide

Several dossiers in ICH CTD format needed to convert to ACTD format. Providers from Asia, but also worldwide, welcome. More »

Looking for a clinical pharmacology expert (Europe)

  • Regulatory services - CMC writing - medical writing
  • Human Medicines
  • Europe

We are looking for a clinical pharmacology expert (Europe), with experience of interacting with the EMA, to provide strategic input into an application for a modified release formulation for a substance that is authorised as an immediate release form... More »

Looking for Consultancy support - vaccine WHO qualification

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

Vaccine to be WHO qualified. Target population being infants. Consultancy firm (Europe, Asia, Africa) should be well versed with EMEA, Article 58, WHO TRSs and all other regulatory implications. More »

Looking for provider for writing and submission type III DMF

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

We are looking for a consultant (Europe) experienced in the writing and submission of type III DMF ( packaging material). More »

Looking for US-based regulatory affairs consultant with oncology and biotech background

  • Clinical development and testing, clinical CRO
  • Biopharmaceuticals
  • North America

We are a EU-based biotech company developing mAb and look for a US based RA consultant who could support us with respect to our programme in order to understand and prepare for US-specific interests, questions and enquiries. We want to be prepared ... More »

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