Regulatory affairs services

Regulatory affairs services
Product Description

I. SERVICES

1. Submission of ANDA, NDA and IND applications with NMPA; (including the whole service from GAP analysis, compiling, submission, sample testing, CDE review procedure tracking and supplemental info preparation);

2. GAP analysis and application strategies setup before the submission to NMPA;

3. Pre-IND/NDA meeting with CDE; (including the preparation, application, tracking and CDE meeting support)

4. API, pharmaceutical excipients and packaging component filling and technical review with CDE;

II. OUR ADVANTAGES

1. Our consultants having a solid background in RA field including more than 10 years of drug registration experiences

2. Obtained more than 30 imported drug registration certificates, more than 7 Phase III clinical trial approval for an innovator. More than 5 Phase I clinical trial approval for a domestic biosimilar product. More than 10 Clinical trial approvals for imported new drugs

3. We have more than 5 experts that from CDE to support our work

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KRB金瑞博

  • Country/Region:
    China
  • On CPHI since:
    2022
  • Employees:
    25 - 49
Company types
Consultancy
View company profile
Categories
more categories Show less

KRB金瑞博

  • Country/Region:
    China
  • On CPHI since:
    2022
  • Employees:
    25 - 49
Company types
Consultancy
View company profile

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