Clinical Supply Management

Clinical Supply Management
Product Description

NerPharMa Srl. offers a wide range of services which includes clinical supply management. Features: it is authorised and has wide experience in the manufacturing, labelling, packaging and distribution of investigational medicinal products from laboratory to production scale for Phase 1 to Phase 4 clinical studies. Its main tasks are packaging design; primary & secondary packaging; drug supply management and worldwide distribution; study randomization; label design and generation; domestic and international shipping; management of returned medication.

NerPharMa srl

  • Country/Region:
    Italy
  • On CPHI since:
    2015
  • Certificates:
    1
  • Employees:
    100 - 249
Company types
Contract Service
Manufacturer/Innovator
Primary activities
Pharmaceutical Company (generic finished products)

NerPharMa srl

  • Country/Region:
    Italy
  • On CPHI since:
    2015
  • Certificates:
    1
  • Employees:
    100 - 249
Company types
Contract Service
Manufacturer/Innovator
Primary activities
Pharmaceutical Company (generic finished products)

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    Product Dosage Form Development Services

    NerPharMa Srl. offers a wide range of services which includes dosage form development services. Features: it can support the development of sterile and oral solid dosage forms (conventional and nonconventional technologies), includes pre-formulation; formulation; process development; clinical supply; scale...

NerPharMa srl resources (1)

  • Brochure A unique CDMO Partner

    NerPharMa is a CDMO with a strong expertise in Oncology, bringing highly potent compounds, new products and unique innovative technologies to the market delivering a wide range of GMP services. NerPharMa owns a wide and cutting-edge organizational structure able to ensure the API full development and production (in NerPharMa DS division) and finished products (in NerPharMa DP division) intended for the world market, as well as the research and development of innovative formulation and delivery systems, operating in accordance with cGMP and are authorized by the most relevant authorities: AIFA, FDA, ANVISA Brazil, China FDA, PMDA Japan and Russia.