Call Us for any Regulatory Support (ectd, fda, EU, MHRA regulatory authorities): +919998661845

Call Us for any Regulatory Support (ectd, fda, EU, MHRA regulatory authorities): +919998661845

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    • Home
    • SERVICES
      • Drug Registration
      • Device Registration
      • Technology Transfer
      • Other Regulatory Services
      • Compliance and Audit
      • Pharmacovigilance
      • Training
    • Software Solution
      • eCTD and NeeS
      • CTD and ACTD
      • RIMS
      • Drug Safety
      • Clinical Trials and BA/BE
    • Regulatory's Links
    • Contact
    • Our affiliated company
  • Home
  • SERVICES
    • Drug Registration
    • Device Registration
    • Technology Transfer
    • Other Regulatory Services
    • Compliance and Audit
    • Pharmacovigilance
    • Training
  • Software Solution
    • eCTD and NeeS
    • CTD and ACTD
    • RIMS
    • Drug Safety
    • Clinical Trials and BA/BE
  • Regulatory's Links
  • Contact
  • Our affiliated company
Pharma Regulatory Submission

Streamline Your Regulatory Journey with Precision eCTD Solutions

Streamline Your Regulatory Journey with Precision eCTD SolutionsStreamline Your Regulatory Journey with Precision eCTD SolutionsStreamline Your Regulatory Journey with Precision eCTD SolutionsStreamline Your Regulatory Journey with Precision eCTD Solutions

Technology Transfer

Technology Transfer

As per WHO Transfer of Technology is defined as “a logical procedure that controls the transfer of any process together with its documentation and professional expertise between development and manufacture or between manufacture sites”. It is a systematic procedure that is followed in order to pass the documented knowledge and experience gained during development and or commercialization to an appropriate, responsible and authorized party. Technology transfer embodies both the transfer of documentation and the demonstrated ability of the receiving unit (RU) to effectively perform the critical elements of the transferred technology, to the satisfaction of all parties and any applicable regulatory bodies.

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