Clinical Department

Clinical Department
Product Description

  • Supervision of IBs, protocols and related documents
  • Initiation and follow-up of clinical trials
  • Selection and contact of CROs

Ascil Biopharm

  • ES
  • 2021
    On CPHI since
  • 1
    Certificates
  • 25 - 49
    Employees
Company types
Manufacturer/Innovator
Primary activities
Analytical Services
Contract Manufacturer
Laboratory Services
Laboratory, Analytical, Biotechnology Equipment
Medical Devices
Packaging & drug delivery
Technology

Ascil Biopharm

  • ES
  • 2021
    On CPHI since
  • 1
    Certificates
  • 25 - 49
    Employees
Company types
Manufacturer/Innovator
Primary activities
Analytical Services
Contract Manufacturer
Laboratory Services
Laboratory, Analytical, Biotechnology Equipment
Medical Devices
Packaging & drug delivery
Technology

More Products from Ascil Biopharm (5)

  • Analytical and Phy-Chem Department

    Product Analytical and Phy-Chem Department

    • Setup and development of analytical methods • Analytical support to formulation and process studies • QC testing of batches involved in in-vivo studies and supervision of bioanalysis • QC Testing of GMP batches • Microbiology (monitoring of GMP Pilot Plant) • Non-G...
  • Formulation, Process & Device Department

    Product Formulation, Process & Device Department

    • Compatibility studies and preformulation • Formulation and lab-scale batches • Definition and supervision of in-vivo studies • Non-GMP and GMP activities • Med-Tech workshop for device prototyping
  • GMP Pilot Plant

    Product GMP Pilot Plant

    • Manufacturing of pilot /scale-up batches • Manufacturing of GMP and clinical batches • Preparation of clinical kits
  • QA Department

    Product QA Department

    • Overall QA system • Internal and external audits
  • QP, Tech Direction and Regulatory

    Product QP, Tech Direction and Regulatory

    • Supervision of GMP activities • Release of GMP and clinical batches • Relationship with agencies • Consolidation and maintenance of regulatory documents