Drug Product Development, CDMA identification and Technology transfer of product

Drug Product Development, CDMA identification and Technology transfer of product
Product Description

Metina supports pharmaceutical company in developing required dosage forms at accredited formulation development laboratory, in line with EU / US reference product. Post development, the product technology would be transferred to suggested manufacturing location.  Metina can also help in identifying contract manufacturing location so as to have product supply. Metina has played key role in developing injectables, topical, and oral solid dosage forms for USA and EU markets. We have multiple manufacturing sites getting EU accreditation, it is easy for us in proceeding further for site identification and technology transfer of the product.

Metina PharmConsulting Private Limited

  • IN
  • 2015
    On CPHI since
Company types
Contract Service

Metina PharmConsulting Private Limited

  • IN
  • 2015
    On CPHI since
Company types
Contract Service

More Products from Metina PharmConsulting Private Limited (2)

  • API EU QP Audit

    Product API EU QP Audit

    Metina provides support to API manufactures one time audit by independent auditor for single API. It provides benefits to the manufactures to conserve company's resources (i.e. cost of travel and stay for buyer specific auditor, one-time engagement of manufacturing and QA personnel), one single QP audit ca...
  • Regulatory Services for small molecules

    Product Regulatory Services for small molecules

    Metina provides end to end regulatory services starting from due diligence, gap analysis of the dossier, product development guidance, regulatory strategy, scientific writing of dossier, submission to health authority, query response and approval. Our services covers API and Formula...

Metina PharmConsulting Private Limited resources (1)